Open AccessA novel mutation in N-terminal actin-binding domain of the DMD gene presenting becker muscular dystrophy as recurrent exertional rhabdomyolysis: A case report
Author(s) -
JongMok Lee
Publication year - 2020
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_215_19
Subject(s) - medicine , rhabdomyolysis , muscular dystrophy , gene , mutation , terminal (telecommunication) , domain (mathematical analysis) , genetics , bioinformatics , biology , computer science , telecommunications , mathematical analysis , mathematics