Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype-Reference-Cited by-同舟云学术

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Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype

Published:2004-03-01 Issue:3 Volume:41 Page:230-232
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bauer P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 85 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. The New Face of Dynamic Mutation—The CAA [CAG]n CAA CAG Motif as a Mutable Unit in the TBP Gene Causative for Spino-Cerebellar Ataxia Type 17;International Journal of Molecular Sciences;2024-07-26

2. Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders;Journal of the Neurological Sciences;2023-08

3. Complex Ataxia‐Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia;Movement Disorders;2023-02-17

4. Genotype–Phenotype Correlations for ATX‐ TBP ( SCA17 ): MDSGene Systematic Review;Movement Disorders;2022-11-14

5. Role of the TATA-box binding protein (TBP) and associated family members in transcription regulation;Gene;2022-07

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