(<scp>TTTCA</scp>)exp Drives the Genotype–Phenotype Correlation and Genetic Anticipation in <scp>FCMTE1</scp>

The (TTTCA)exp insertion serves as the length-dependent pathogenic component within the two-motif repeat expansion. Its differential expanding nature during parental transmissions is highly associated with the genetic anticipation in FCMTE1. © 2024 International Parkinson and Movement Disorder Society.

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Publication Details

Journal
Movement Disorders
Published
2024-11-21
DOI
https://doi.org/10.1002/mds.30057
Citations
1
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
0.55

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article

(TTTCA)exp Drives the Genotype–Phenotype Correlation and Genetic Anticipation in FCMTE1

Shuang Wang, Lebo Wang, Yao Ding, Ben Hu et al.
1 citations
Movement Disorders
Genetics and Neurodevelopmental Disorders
0.55
article

(TTTCA)exp Drives the Genotype–Phenotype Correlation and Genetic Anticipation in FCMTE1

Shuang Wang, Lebo Wang, Yao Ding, Ben Hu, Dehao Yang, Zhidong Cen, Yiling Elaine Chen, Yixin Kang, Huijun Yu, Haibin Xia, Nan Jin, Sheng Wu, Wei Luo, Peng Liu, Miao Chen, Haotian Wang, Fan Zhang, Bo Wang, Fei Xie, Xinhui Chen, Aisi Fu, Zhiyuan Ouyang, Junfeng Ji
article en
1 citations

Abstract

The (TTTCA)exp insertion serves as the length-dependent pathogenic component within the two-motif repeat expansion. Its differential expanding nature during parental transmissions is highly associated with the genetic anticipation in FCMTE1. © 2024 International Parkinson and Movement Disorder Society.

Movement DisordersVol. 40(2)
Wenzhou Medical University (CN), Sir Run Run Shaw Hospital (CN), Wuhan University (CN), Zhongnan Hospital of Wuhan University (CN), Third People's Hospital of Hangzhou (CN), Taizhou Central Hospital (CN), Second Affiliated Hospital of Zhejiang University (CN), Zhejiang University (CN), Taizhou University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province, Science and Technology Program of Zhejiang Province
Openalex Percentile: Top 24%
Genetics and Neurodevelopmental Disorders
0.55
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