Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy-Reference-Cited by-同舟云学术

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Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy

Published:2016-11-21 Issue:1 Volume:3 Page:e123
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Takahashi Yuji,Kanai Masahiro,Taminato Tomoya,Watanabe Shoko,Matsumoto Chihiro,Araki Toshiyuki,Okamoto Tomoko,Ogawa Masafumi,Murata Miho

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),Clinical Neurology

Reference7 articles.

1. Toward understanding Machado–Joseph disease

2. Population Genetics of Wild-Type CAG Repeats in the Machado-Joseph Disease Gene in Portugal

3. Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population;Gan;PLoS one,2015

4. Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals;Freund;Arq Neuropsiquiatr,2009

5. The shortest expanded allele of the MJD1 gene in a Chinese MJD kindred with autonomic dysfunction;Gu;Eur Neurol,2004

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1. Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China;2023-05-15

2. Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population;Acta Neuropathologica Communications;2020-11-09

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