Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H. (Q34405791)

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English	Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

title

Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

author

Benedikt Schoser

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

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9 January 2020

Patrick Frosk

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2

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stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

Hanns Lochmüller

series ordinal

5

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Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

author name string

Andrew G Engel

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

Ursula Klutzny

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

Klaus Wrogemann

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

publication date

1 April 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

published in

Annals of Neurology

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Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

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9 January 2020

volume

57

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Europe PubMed Central

PubMed publication ID

15786463

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

issue

4

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Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

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9 January 2020

page(s)

591-595

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Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

cites work

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

The tripartite motif family identifies cell compartments

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

RING protein Trim32 associated with skin carcinogenesis has anti-apoptotic and E3-ubiquitin ligase properties

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

Cytochemistry of phosphatases of the sarcoplasmic reticulum. II. In situ localization of the Mg-dependent enzyme

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.20441

retrieved

21 January 2018

Identifiers

DOI

10.1002/ANA.20441

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

PubMed publication ID

15786463

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15786463

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 January 2020

 

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