Co‐occurrence of ATXN3 and ATXN2 repeat expansions in Chinese ataxia patients with slow saccades-Reference-Cited by-同舟云学术

Co‐occurrence of ATXN3 and ATXN2 repeat expansions in Chinese ataxia patients with slow saccades

Published:2019-03-28 Issue: Volume: Page:e663
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Wu Chao¹^ORCID,Cai Qiong¹,You Huajing¹,Zhou Xiangxue²^ORCID,Chen Dingbang¹,Mo Guiling³,Li Xunhua¹

Affiliation:

1. Department of Neurology, National Key Clinical Department and Key Discipline of Neurology The First Affiliated Hospital, Sun Yat‐sen University Guangzhou China

2. Department of Neurology The East Area of the First Affiliated Hospital, Sun Yat‐sen University Guangzhou Guangdong China

3. Guangzhou KingMed Center for Clinical Laboratory Co. Ltd Guangzhou Guangdong China

Funder

The Southern China International Cooperation Base for Early Intervention and Functional Rehabilitation of Neurological Diseases

Guangdong Provincial Key Laboratory for Diagnosis and Treatment of Major Neurological Diseases

Guangdong Provincial Translational Medicine Innovation Platform for Diagnosis and Treatment of Major Neurological Disease

Guangdong Provincial Engineering Center for Major Neurological Disease Treatment

Guangdong Provincial Science and Technology Program

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.663

Reference19 articles.

1. Autosomal dominant cerebellar ataxias: Imaging biomarkers with high effect sizes

2. (CAG) n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China

3. An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia

4. Late-onset SCA2: 33 CAG repeats are sufficient to cause disease

5. Genetic analysis of age at onset variation in spinocerebellar ataxia type 2

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2. Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool;Advanced Genetics;2022-03-10

3. Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias;Parkinsonism & Related Disorders;2021-08

4. Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16;International Journal of Molecular Sciences;2021-05-30