Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.

Name: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.
Author: Rydning, Siri L

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis. — المؤلف: Rydning, Siri L — Brain : a journal of neurology 20191206

المؤلف: Rydning, Siri L
النشر: Brain : a journal of neurology 20191206
الوصف: e12 p.
الموضوعات: Humans؛ Intellectual Disability؛ Muscle Spasticity؛ Mutation؛ Optic Atrophy؛ Paraparesis, Spastic؛ RNA Polymerase III؛ Spinocerebellar Ataxias