Mutation analysis of cerebrotendinous xanthomatosis in an Indian case-Reference-Cited by-同舟云学术

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Mutation analysis of cerebrotendinous xanthomatosis in an Indian case

Published:2012 Issue:6 Volume:60 Page:643
ISSN:0028-3886
Container-title:Neurology India
language:en
Short-container-title:Neurol India

Author:

Shah Krati,Mathew Vivek,Gallus GianNicola,Dotti MariaTeresa,Federico Antonio,Danda Sumita

Publisher

Medknow

Subject

Neurology (clinical),Neurology

Cited by 3 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. A novel CYP27A1 frameshift mutation causing cerebrotendinous xanthomatosis in an Indian family;Annals of Movement Disorders;2022-05

2. First case series of Polish patients with cerebrotendinous xanthomatosis and systematic review of cases from the 21st century;Clinical Genetics;2021-11-24

3. Cerebrotendinous xanthomatosis: Possibility of founder mutation in CYP27A1 gene (c.526delG) in Eastern Indian and Surinamese population;Molecular Genetics and Metabolism Reports;2015-06

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