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

✍ Scribed by M. Li; K. Ishikawa; S. Toru; H. Tomimitsu; M. Takashima; J. Goto; Y. Takiyama; H. Sasaki; I. Imoto; J. Inazawa; T. Toda; I. Kanazawa; H. Mizusawa

Book ID: 106252869
Publisher: Nature Publishing Group
Year: 2003
Tongue: English
Weight: 336 KB
Volume: 48
Category: Article
ISSN: 1435-232X
DOI: 10.1007/s100380300017

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## Abstract Autosomal dominant spinocerebellar ataxias (AD‐SCAs) form a clinically and genetically heterogeneous group of neurodegenerative disorders. Recently, a single nucleotide substitution in the 5′‐untranslated region of the __puratrophin‐1__ gene was found to be associated with one type of A