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Intractable epilepsy of infancy due to homozygous mutation in the EFHC1 gene.

Authors
Type
Published Article
Journal
Epilepsia
Publication Date
Volume
53
Issue
8
Pages
1436–1440
Identifiers
DOI: 10.1111/j.1528-1167.2012.03536.x
PMID: 22690745
Source
Medline

Abstract

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