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Article

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.

Journal of human genetics - 1 Jan 2003

Li Mingshun, Ishikawa Kinya, Toru Shuta, Tomimitsu Hiroyuki, Takashima Minoru, Goto Jun, Takiyama Yoshihisa, Sasaki Hidenao, Imoto Issei, Inazawa Johji, Toda Tatsushi, Kanazawa Ichiro, Mizusawa Hidehiro

Abstract excerpt

Autosomal dominant cerebellar ataxia (ADCA) is a group of heterogeneous neurodegenerative disorders. We previously mapped a gene locus for ADCA with pure cerebellar syndrome (ADCA type III) to a 3-cM region in chromosome 16q, and found a common haplotype among affected individuals. This region was exactly within the locus for another ADCA, spinocerebellar ataxia type 4 (SCA4). To identify the gene causing...

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Identifiers

PMID: 12624721
DOI: 10.1007/s100380300017

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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