SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
Autor: | Patel H, Cross H, Proukakis C, Hershberger R, Peer Bork, Fd, Ciccarelli, Ma, Patton, Va, Mckusick, Ah, Crosby |
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Zdroj: | Europe PubMed Central |
Databáze: | OpenAIRE |
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