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Familial cerebral cavernous malformation presenting with epilepsy caused by mutation in the CCM2 gene
Author(s) -
Kazuhiro Ishii,
Naoki Tozaka,
Satoshi Tsutsumi,
Ai Muroi,
Akira Tamaoka
Publication year - 2020
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000019800
Subject(s) - medicine , levetiracetam , hemangioma , epilepsy , mutation , magnetic resonance imaging , occipital lobe , neurology , pathology , gene mutation , gene , genetics , radiology , biology , psychiatry

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