First report of a Mongolian family with spinocerebellar ataxia type I-Reference-Cited by-同舟云学术

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First report of a Mongolian family with spinocerebellar ataxia type I

Published:2019-05 Issue:5 Volume:118 Page:951-952
ISSN:0929-6646
Container-title:Journal of the Formosan Medical Association
language:en
Short-container-title:Journal of the Formosan Medical Association

Author:

Chuluunbat Munkhzaya,Tsagaankhuu Delgermaa,Tang Sung-Chun,Enkhsaikhan Lhamsuren

Funder

First Central Hospital of Mongolia, Mongolia

National Taiwan University Hospital, Taiwan

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol,2010

2. Hereditary ataxias: overview;Jayadev;Genet Med: Off J American Coll Med Genet,2013

3. Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1;Martins Junior;Arquivos de neuro-psiquiatria,2018

4. Autosomal dominant hereditary ataxia in Sri Lanka;Sumathipala;BMC Neurol,2013

5. Clinical analysis of adult-onset spinocerebellar ataxias in Thailand;Boonkongchuen;BMC Neurol,2014

Cited by 1 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. Spinocerebellar ataxias in Asia: Prevalence, phenotypes and management;Parkinsonism & Related Disorders;2021-11

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