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A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia
Author(s) -
Faber I.,
Prota J. R. M.,
Martinez A. R. M.,
LopesCendes I.,
França M. C.
Publication year - 2017
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/ene.13194
Subject(s) - medical school , medicine , hereditary spastic paraplegia , humanities , phenotype , medical education , art , biology , genetics , gene
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