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NBIA due to FA2H gene mutations is allelic with hereditary spastic paraplegia (SPG35) and a form of familial leukodystrophy
Author(s) -
Schneider Susanne A.
Publication year - 2011
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.23715
Subject(s) - hereditary spastic paraplegia , leukodystrophy , genetics , medicine , psychology , gene , biology , pathology , phenotype , disease
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