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Autosomal Recessive Spinocerebellar Ataxia 19
An autosomal recessive cerebellar ataxia that is characterized by postnatal onset of severe progressive sensorineural hearing loss and progressive cerebellar ataxia and that is caused by homozygous mutation in the SLC9A1
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Overview
An autosomal recessive cerebellar ataxia that is characterized by postnatal onset of severe progressive sensorineural hearing loss and progressive cerebellar ataxia and that is caused by homozygous mutation in the SLC9A1
Resources
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