Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

BACKGROUND: Congenital nonprogressive spinocerebellar ataxia is characterized by early gross motor delay, hypotonia, gait ataxia, mild dysarthria and dysmetria. The clinical presentation remains fairly stable and may be associated with cerebellar atrophy. To date, only a few families with autosomal...

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Detalles Bibliográficos
Autores principales: Huang, Lijia, Chardon, Jodi Warman, Carter, Melissa T, Friend, Kathie L, Dudding, Tracy E, Schwartzentruber, Jeremy, Zou, Ruobing, Schofield, Peter W, Douglas, Stuart, Bulman, Dennis E, Boycott, Kym M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545966/
https://www.ncbi.nlm.nih.gov/pubmed/22986007
http://dx.doi.org/10.1186/1750-1172-7-67

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545966/
https://www.ncbi.nlm.nih.gov/pubmed/22986007
http://dx.doi.org/10.1186/1750-1172-7-67

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