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Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
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Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia. J Hum Genet. 2007; 52(8):643-649.
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PubMed
subject areas
Cerebellar Ataxia
Chromosome Mapping
Chromosomes, Human, Pair 16
Genes, Dominant
Genetic Linkage
Guanine Nucleotide Exchange Factors
Haplotypes
Humans
Polymorphism, Single Nucleotide
Spectrin