Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males (Q57206738)

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scientific article published in The Lancet

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Language	Label	Description	Also known as
English	Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males	scientific article published in The Lancet

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

title

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

main subject

neurodevelopmental disorder

1 reference

based on heuristic

inferred from title

author

Graeme Black

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

author name string

J Clayton-Smith

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

P Watson

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

S Ramsden

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

language of work or name

English

0 references

publication date

1 September 2000

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

published in

The Lancet

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

volume

356

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

issue

9232

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

page(s)

830-832

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

cites work

Rett syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Rett syndrome in a boy with a 47,XXY karyotype

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0140-6736(00)02661-1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

PubMed publication ID

11022934

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11022934

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json

retrieved

31 October 2019

 

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