Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families-Reference-Cited by-同舟云学术

Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families

Published:2015-04-04 Issue:5 Volume:30 Page:743-744
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Ma Ling-Yan¹²,Wang Lin²,Yang Ying-Mai²,Feng Tao¹,Wan Xin-Hua²

Affiliation:

1. Center for Neurodegenerative disease, Department of Neurology; Beijing Tiantan Hospital, Capital Medical University; Beijing People's Republic of China

2. Department of Neurology; Peking Union Medical College Hospital, Chinese Academy of Medical Sciences; Beijing People's Republic of China

Funder

Natural Science Foundation of Beijing China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.26190/fullpdf

Reference5 articles.

1. Phenomenology and classification of dystonia: a consensus update;Albanese;Mov Disord,2013

2. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am J Hum Genet,2012

3. Mutations in GNAL cause primary torsion dystonia;Fuchs;Nat Genet,2013

4. Mutations in GNAL: a novel cause of craniocervical dystonia;Kumar;JAMA Neurol,2014

5. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls;Zech;Mov Disord,2014

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1. The expanding clinical and genetic spectrum of ANO3 dystonia;Neuroscience Letters;2021-02

2. Isolated dystonia: clinical and genetic updates;Journal of Neural Transmission;2020-11-27

3. ANO3 Mutations in Chinese Dystonia: A Genetic Screening Study Using Next-Generation Sequencing;Frontiers in Neurology;2020-02-07

4. Dystonia genes and their biological pathways;Neurobiology of Disease;2019-09

5. Novel anoctamin-3 missense mutation responsible for early-onset myoclonic dystonia;Parkinsonism & Related Disorders;2019-07