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A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings

Detalles Bibliográficos
Autores principales:	Chakravarty, Kamalesh, Lal, Vivek, Ray, Sucharita
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2021
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513945/ https://www.ncbi.nlm.nih.gov/pubmed/34728966 http://dx.doi.org/10.4103/aian.AIAN_970_20

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