SCN4A (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "SCN4A" in French language version.

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ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000007314 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000001027 - Ensembl, May 2017

neurology.org

n.neurology.org

Lion-Francois L, Mignot C, Vicart S et al. Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder, Neurology, 2010;75:641–645

nih.gov

ncbi.nlm.nih.gov

« Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
« Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine

oup.com

academic.oup.com

Zaharieva IT, Thor MG, Oates EC et al. Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’ congenital myopathy, Brain, 2016;139:674–691

pnas.org

Tsujino A, Maertens C, Ohno K et al. Myasthenic syndrome caused by mutation of the SCN4A sodium channel, Proc Natl Acad Sci USA, 2003;100:7377–7382

thelancet.com

Männikkö R, Wong L, Tester DJ et al. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study, Lancet, 2018;391:1483–1492

wiley.com

onlinelibrary.wiley.com

Cannon SC, Channelopathies of skeletal muscle excitability, Compr Physiol, 2015;5:761–790
Gay S, Dupuis D, Faivre L et al. Severe neonatal non-dystrophic myotonia secondary to a novel mutation of the voltage-gated sodium channel (SCN4A) gene, Am J Med Genet A, 2008;146:380–383