TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study-Reference-Cited by-同舟云学术

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TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study

Published:2021-05 Issue: Volume:779 Page:145495
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Cheng Hao-Ling,Dong Hai-Lin,Liu De-Shan,Ni Wang,Ma Yin,Yang Lu,Du Yi-Chu,Chen Dian-Fu,Dong Yi,Wu Zhi-Ying

Funder

Zhejiang University

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference31 articles.

1. The MFN2 V705I variant is not a disease-causing mutation: a segregation analysis in a cmt2 family;Albulym;J. Neurodegener. Dis.,2013

2. MFN2 point mutations occur in 3.4% of charcot-marie-tooth families. An investigation of 232 norwegian cmt families;Braathen;BMC Med. Genet.,2010

3. LRP10 in autosomal-dominant Parkinson's disease;Chen;Mov. Disord.,2019

4. Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration;Chen;Park. Relat. Disord.,2018

5. TGM6 L517W is not a pathogenic variant for spinocerebellar ataxia type 35;Chen;Neurol. Genet.,2020

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 Ataxia Type 35 Caused by a New TGM6 Variant: Video Documentation of a German Family;Movement Disorders Clinical Practice;2023-03-27

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