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Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified
Author(s) -
Kaur A
Publication year - 2013
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12239
Subject(s) - epilepsy , mutation , genetics , biology , neuroscience , gene
Mutations in DEPDC5 cause familial focal epilepsy with variable foci Dibbens et al. (2013) Nature Genetics 45: 546–551. Mutations of DEPDC5 cause autosomal dominant focal epilepsies Ishida et al. (2013) Nature Genetics 45: 552–555.
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