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Article

Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A.

Neurology - 24 Jan 2017

Mercier Sandra, Lornage Xavière, Malfatti Edoardo, Marcorelles Pascale, Letournel Franck, Boscher Cécile, Caillaux Gaëlle, Magot Armelle, Böhm Johann, Boland Anne, Deleuze Jean-François, Romero Norma, Péréon Yann, Laporte Jocelyn

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28003497
DOI: 10.1212/WNL.0000000000003535
PMCID: PMC5272967

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