Open AccessResponse to the paper titled "Identification of a novel <em>CACNA1A</em> mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy"
Author(s) -
Tracey D. Graves
Publication year - 2018
Publication title -
neuropsychiatric disease and treatment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 67
eISSN - 1178-2021
pISSN - 1176-6328
DOI - 10.2147/ndt.s179068
Subject(s) - medicine , chinese family , genetics , mutation , gene , biology
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