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ArticleAnnals of Indian Academy of Neurology

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

Kamalesh Chakravarty et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2025
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Full record →Abstract, authors, funding and every citing paper · PMID 34728966