A novel mutation in the CLCN1 gene causing autosomal recessive myotonia congenita in siblings

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Bibliographic Details
Published inAnnals of the Indian Academy of Neurology Vol. 24; no. 4; pp. 605 - 606
Main Authors Chakravarty, Kamalesh, Lal, Vivek, Ray, Sucharita
Format Journal Article
LanguageEnglish
Published Mumbai Wolters Kluwer India Pvt. Ltd 01.07.2021
Medknow Publications & Media Pvt. Ltd
Wolters Kluwer - Medknow
Wolters Kluwer Medknow Publications
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Myotonia
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Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0972-2327
1998-3549
DOI:10.4103/aian.AIAN_970_20