Genetic and clinical features of Chinese patients with mitochondrial ataxia identified by targeted next‐generation sequencing-Reference-Cited by-同舟云学术

Genetic and clinical features of Chinese patients with mitochondrial ataxia identified by targeted next‐generation sequencing

Published:2018-05-13 Issue:1 Volume:25 Page:21-29
ISSN:1755-5930
Container-title:CNS Neuroscience & Therapeutics
language:en
Short-container-title:CNS Neurosci Ther

Author:

Dong Hai‐Lin¹,Ma Yin¹,Li Quan‐Fu¹,Du Yi‐Chu¹,Yang Lu¹,Chen Sheng²,Wu Zhi‐Ying¹^ORCID

Affiliation:

1. Department of Neurology and Research Center of Neurology in Second Affiliated Hospital Key Laboratory of Medical Neurobiology of Zhejiang Province Zhejiang University School of Medicine Hangzhou China

2. Department of Neurology Huashan Hospital Shanghai Medical College Fudan University Shanghai China

Funder

Zhejiang University

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cns.12972

Reference49 articles.

1. Spinocerebellar ataxia: relationship between phenotype and genotype - a review

2. Sporadic ataxia with adult onset: classification and diagnostic criteria

3. Mitochondrial pathology in progressive cerebellar ataxia

4. Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients

5. Adult-onset spinocerebellar ataxia due to MTATP6 mutations: are they more common than previously thought?

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