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Late‐onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations
Author(s) -
Lee H.N.,
Koh S.H.,
Lee K.Y.,
Ki C.S.,
Lee Y. J.
Publication year - 2009
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/j.1468-1331.2008.02395.x
Subject(s) - medicine , compound heterozygosity , white matter , genetics , disease , gene , mutation , magnetic resonance imaging , biology , radiology