Spinocerebellar ataxia subtype 40: Report of a case and review of literature-Reference-Cited by-同舟云学术

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Spinocerebellar ataxia subtype 40: Report of a case and review of literature

Published:2024-06 Issue: Volume:123 Page:106957
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Kale Gautam Bhausaheb,Rangnathan Prajnya,Divate Pradeep,Murthy J.M.K.^ORCID

Publisher

Elsevier BV

Reference13 articles.

1. Molecular pathogenesis of spinocerebellar ataxias;Duenas;Brain,2006

2. A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia;Tsoi;J. Med. Genet.,2014

3. Familial ataxia tremor and dementia in a polish family with a novel mutation in the CCDC88C gene;Leńska-Mieciek;Mov. Disord.,2019

4. Spinocerebellar ataxia 40: another etiology underlying essential tremor syndrome;Emamikhah;Mov. Disord. Clin. Pract.,2021

5. Spinocerebellar ataxia type 40: a case report and literature review;Han;Transl. Neurosci.,2021

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