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Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation
Author(s) -
Mir Ali,
Hadab Safeya,
Sammak Mohammed,
Alhazmi Rami,
Housawi Yousef,
Bashir Shahid
Publication year - 2020
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.13763
Subject(s) - vigabatrin , mutation , medicine , epilepsy , pediatrics , genetics , gene , biology , anticonvulsant , psychiatry
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