Advances in Sequencing Technologies for Understanding Hereditary Ataxias-Reference-Cited by-同舟云学术

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Advances in Sequencing Technologies for Understanding Hereditary Ataxias

Published:2016-12-01 Issue:12 Volume:73 Page:1485
ISSN:2168-6149
Container-title:JAMA Neurology
language:en
Short-container-title:JAMA Neurol

Author:

Didonna Alessandro¹,Opal Puneet²

Affiliation:

1. Department of Neurology, University of California, San Francisco

2. Davee Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois3Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

Cited by 18 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. Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report;Frontiers in Genetics;2023-07-06

2. Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on Biomarkers;The Cerebellum;2023-05-27

3. Autism Spectrum Disorders and Ataxia;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05

4. Spinocerebellar ataxia clinical trials: opportunities and challenges;Annals of Clinical and Translational Neurology;2021-05-21

5. Genetics in Movement Disorder Phenomenology;Movement Disorders Phenomenology;2020

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