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Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)
Katherine J. Dick, Matthias Eckhardt, Coro Paisán-Ruiz, Aisha Alkhayat Alshehhi, Christos Proukakis, Naomi A. Sibtain, Helena Maier, Reza Sharifi, Michael A. Patton, Wafa Bashir, Roshan Koul, Sandy RaVolume:
31
Année:
2010
Langue:
english
Pages:
1
DOI:
10.1002/humu.21205
Fichier:
PDF, 563 KB
english, 2010