Homozygosity Mapping of Spinocerebellar Ataxia With Cerebellar Atrophy and Peripheral Neuropathy to 9q33–34, and With Hearing Impairment and Optic Atrophy to 6p21–23

European Journal of Human Genetics - United Kingdom
doi 10.1038/sj.ejhg.5200586
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Genetics
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Springer Science and Business Media LLC