Literature DB >> 11266690

Spinocerebellar ataxia type 6: founder effect in Western Japan.

M Mori1, Y Adachi, M Kusumi, K Nakashima.   

Abstract

An accumulation of SCA6 cases has been observed in the Chugoku area of Western Japan. In the Tottori prefecture, located in the northeastern part of the Chugoku district, we observed a cluster of SCA6 families within the eastern area, suggesting that there may be a founder in the Japanese SCA6 population. Genotyping with DNA microsatellite markers linked to the CACNL1A4 gene on chromosome 19p13 demonstrated shared allelic characteristics and revealed a common haplotype in the majority of Japanese families. The common haplotype of the shared (CAG)(22) repeat found in this study may indicate the meiotic stability of CAG repeats in SCA6 patients.

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Year:  2001        PMID: 11266690     DOI: 10.1016/s0022-510x(01)00453-1

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  1 in total

1.  Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.

Authors:  Dineke S Verbeek; Bart P C van de Warrenburg; F A M Hennekam; Dennis Dooijes; P F Ippel; Corien C Verschuuren-Bemelmans; H P H Kremer; Richard J Sinke
Journal:  Hum Genet       Date:  2005-04-20       Impact factor: 4.132

  1 in total

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