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A Case of a 6-Year-old Girl with a Rare Compound Heterozygous Mutation of KCTD7 Presenting with Progressive Myoclonic Epilepsy

Reza Shervin Badv, Fakhreddin Shariatmadari,Shiva Bayat,Sara Memarian, Samaneh Esteghamat Hanzae, Hossein Yousefimanesh

EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS（2024）

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关键词
KCTD7,Epilepsy,Mutation
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