A novel mutation in the CLCN1 gene causing autosomal recessive myotonia congenita in siblings
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2021-01-01
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Series: | Annals of Indian Academy of Neurology |
Online Access: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2021;volume=24;issue=4;spage=605;epage=606;aulast=Chakravarty |