A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS. (Q48005273)

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scientific article published on 5 January 2017

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English	A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS.	scientific article published on 5 January 2017

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scholarly article

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Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

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http://europepmc.org/abstract/MED/28054830

title

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

main subject

amyotrophic lateral sclerosis

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author

Helene Blasco

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Helene Blasco

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7

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Christian Andres

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Christian Andres

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5

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Philippe Corcia

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1

object named as

Philippe Corcia

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

Patrick Vourc'H

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8

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Patrick Vourc'h

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

Arnaud Lacour

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3

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Arnaud Lacour

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Europe PubMed Central

PubMed publication ID

28054830

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7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

Veronique Danel

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2

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Veronique Danel

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Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

Stephane Beltran

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4

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Stephane Beltran

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Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

Philippe Couratier

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6

object named as

Philippe Couratier

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

publication date

5 January 2017

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stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

published in

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

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stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

volume

18

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stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

issue

3-4

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stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

page(s)

298-301

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Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

cites work

Natural history of young-adult amyotrophic lateral sclerosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

Incidence of amyotrophic lateral sclerosis in Europe

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

FUS-NLS/Transportin 1 complex structure provides insights into the nuclear targeting mechanism of FUS and the implications in ALS

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F21678421.2016.1265564

retrieved

21 January 2018

Identifiers

DOI

10.1080/21678421.2016.1265564

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

PubMed publication ID

28054830

1 reference

stated in

Europe PubMed Central

PubMed publication ID

28054830

retrieved

7 February 2018

reference URL

http://europepmc.org/abstract/MED/28054830

 

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