Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease-Reference-Cited by-同舟云学术

Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease

Published:2024-01 Issue:1 Volume:111 Page:82-95
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Wallenius Joel,Kafantari Efthymia,Jhaveri Emma,Gorcenco Sorina,Ameur Adam,Karremo Christin,Dobloug Sigurd,Karrman Kristina,de Koning Tom,Ilinca Andreea,Landqvist Waldö Maria,Arvidsson Andreas,Persson Staffan,Englund Elisabet,Ehrencrona Hans,Puschmann Andreas^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference45 articles.

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2. Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia;Pellerin;N. Engl. J. Med.,2023

3. Overview of the Clinical Approach to Individuals With Cerebellar Ataxia and Neuropathy;Roberts;Neurol. Genet.,2022

4. Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?;Wictorin;Parkinsonism Relat. Disorders,2014

5. HLA--determination in families with hereditary ataxia;Möller;Tissue Antigens,1978

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3. Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity;Journal of Neurology;2024-08-02

4. Short Tandem Repeats in the era of next-generation sequencing: from historical loci to population databases;European Journal of Human Genetics;2024-07-10

5. Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs;Journal of Internal Medicine;2024-07-07