Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation-Reference-Cited by-同舟云学术

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Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

Published:2000-02 Issue:2 Volume:106 Page:179-187
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Saleem Q.,Choudhry S.,Mukerji M.,Bashyam L.,Padma M.V.,Chakravarthy A.,Maheshwari M.C.,Jain S.,Brahmachari S.K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390000240.pdf

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unraveling movement disorders in spinocerebellar ataxia;Annals of Movement Disorders;2022-05

2. Clinical and Molecular Spectrum of Degenerative Cerebellar Ataxia: A Single Centre Study;Neurology India;2022

3. Autosomal Dominant Spinocerebellar Ataxias and Episodic Ataxias;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05

4. Spinocerebellar ataxias in Asia: Prevalence, phenotypes and management;Parkinsonism & Related Disorders;2021-11

5. SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series;Parkinsonism & Related Disorders;2021-08

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