Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy (Q21560937)

GOA release 2020-03-11

13

Ana Ferreiro

Ana

Ferreiro

1 reference

15 September 2022

11

Valérie Allamand

Valérie

Allamand

1 reference

15 September 2022

3

Sandrine Arbogast

Sandrine

Arbogast

1 reference

15 September 2022

12

Pascale Guicheney

Pascale

Guicheney

1 reference

15 September 2022

Mathieu Rederstorff

1

Mathieu

Rederstorff

1 reference

15 September 2022

Stéphane Vassilopoulos

object named as

Stéphane Vassilopoulos

5

Stéphane

Vassilopoulos

1 reference

15 September 2022

Perrine Castets

2

Perrine

Castets

1 reference

15 September 2022

Jeanne Lainé

4

Jeanne

Lainé

1 reference

15 September 2022

Maud Beuvin

6

Maud

Beuvin

1 reference

15 September 2022

Odile Dubourg

7

Odile

Dubourg

1 reference

15 September 2022

Alban Vignaud

8

Alban

Vignaud

1 reference

15 September 2022

Arnaud Ferry

9

Arnaud

Ferry

1 reference

15 September 2022

Alain Krol

10

Alain

Krol

1 reference

15 September 2022

Alain Lescure

14

Alain

Lescure

1 reference

Creative Commons Attribution 4.0 International

15 September 2022

language of work or name

English

0 references

publication date

2011

0 references

published in

PLOS One

0 references

volume

6

0 references

issue

8

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page(s)

e23094

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copyright license

start time

8 August 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

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Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies

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29 November 2018

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29 November 2018

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29 November 2018

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29 November 2018

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29 November 2018

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1 reference

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inferred from PubMed ID database lookup

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The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21858002

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0023094

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