Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

Hereditary spastic paraplegia (HSP) comprises a group of clinically and genetically heterogeneous diseases that affect the upper motor neurons and their axonal projections. For the novel SPG31 locus on chromosome 2p12, we identified six different mutations in the receptor expression–enhancing protei...

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Main Authors: Züchner, Stephan, Wang, Gaofeng, Tran-Viet, Khanh-Nhat, Nance, Martha A., Gaskell, Perry C., Vance, Jeffery M., Ashley-Koch, Allison E., Pericak-Vance, Margaret A.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1559498/
https://ncbi.nlm.nih.gov/pubmed/16826527
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