Open AccessA novel mutation in the clcn1 gene causing autosomal recessive myotonia congenita in siblings
Author(s) -
Kamalesh Chakravarty,
Vivek Lal,
Sucharita Ray
Publication year - 2021
Publication title -
annals of indian academy of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_970_20
Subject(s) - myotonia congenita , medicine , genetics , mutation , gene , myotonia , biology , myotonic dystrophy