Mutation analysis of the TATA box-binding protein (TBP) gene in Russian patients with spinocerebellar ataxia and Huntington disease-like phenotype-Reference-Cited by-同舟云学术

Mutation analysis of the TATA box-binding protein (TBP) gene in Russian patients with spinocerebellar ataxia and Huntington disease-like phenotype

Published:2022-11 Issue: Volume:222 Page:107473
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Ivanova Ekaterina,Nuzhnyi Evgenii,Abramycheva Natalia,Klyushnikov Sergey,Fedotova Ekaterina,Illarioshkin Sergey

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Surgery

Reference16 articles.

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3. Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4);Stevanin;Cerebellum,2008

4. Complexity of the genetics and clinical presentation of spinocerebellar Ataxia 17;Nethisinghe;Front. Cell Neurosci.,2018

5. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia;Fujigasaki;Brain,2001

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