Spinocerebellar Ataxia 21 with Retardation

Abstract

Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.

Keywords

• neurology
• pediatrics
• child development
• nervous system diseases
• brain diseases