Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome

BACKGROUND: The etiology of many cases of childhood-onset chorea remains undetermined, although advances in genomics are revealing both new disease-associated genes and variant phenotypes associated with known genes. METHODS: We report a Saudi family with a neurodegenerative course dominated by prog...

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Detalles Bibliográficos
Autores principales: Salih, Mustafa A., Seidahmed, Mohammed Z., El Khashab, Heba Y., Hamad, Muddathir H. A., Bosley, Thomas M., Burn, Sabrina, Myers, Angela, Landsverk, Megan L., Crotwell, Patricia L., Bilguvar, Kaya, Mane, Shrikant, Kruer, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2015
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502426/
https://www.ncbi.nlm.nih.gov/pubmed/26203402
http://dx.doi.org/10.7916/D8D21WQ0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502426/
https://www.ncbi.nlm.nih.gov/pubmed/26203402
http://dx.doi.org/10.7916/D8D21WQ0

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