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Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation
Author(s) -
Yoon W. T.,
Lee W. Y.,
Lee S.T.,
Ahn J. Y.,
Ki C.S.,
Cho J. W.
Publication year - 2012
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.1468-1331.2011.03569.x
Subject(s) - medicine , neurology , medical school , center (category theory) , hereditary spastic paraplegia , medical education , psychiatry , genetics , chemistry , biology , phenotype , gene , crystallography