Novel Mutation in Myh7 Gene Causing Scapuloperoneal Syndrome

AuthID
 P-00T-89D
10
Author(s)
Bras, A
·
Rebelo, O
·
Matos, A
·
Geraldo, A
·
Lourenco, M
·
Laranjeiro, F
·
Marmiesse, A
·
Marques, C
·
Negrao, L
Tipo de Documento
Abstract
Year published
2017
Publicado
in NEUROLOGY, ISSN: 0028-3878
Volume: 88
Indexing
Wos®
Publication Identifiers
Wos: WOS:000577381502363
Source Identifiers
ISSN: 0028-3878
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