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

@article{Li2003PhysicalMA,
  title={Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan},
  author={Mingshun Li and Kinya Ishikawa and Shuta Toru and Hiroyuki Tomimitsu and Minoru Takashima and Jun Goto and Yoshihisa Takiyama and Hidenao Sasaki and Issei Imoto and Johji Inazawa and Tatsushi Toda and Ichiro Kanazawa and Hidehiro Mizusawa},
  journal={Journal of Human Genetics},
  year={2003},
  volume={48},
  pages={111-118}
}
AbstractAutosomal 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 16q-linked ADCA type III, we constructed a contig with 38 bacterial artificial… CONTINUE READING

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