Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS-Reference-Cited by-同舟云学术

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Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS

Published:2016-09-30 Issue:17 Volume:87 Page:1763-1769
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Liu Qing,Shu Shi,Wang Rong Rong,Liu Fang,Cui Bo,Guo Xia Nan,Lu Chao Xia,Li Xiao Guang,Liu Ming Sheng,Peng Bin,Cui Li-ying,Zhang Xue

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 68 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analysis of clinical and gene mutation characteristics in patients of isolated myopathy caused by <italic>HNRNPA1</italic> mutation;SCIENTIA SINICA Vitae;2024-08-01

2. Dominant stop‐loss HNRNPA1 variants in juvenile‐onset myopathy;Muscle & Nerve;2024-07-28

3. Genotype-phenotype association and functional analysis of hnRNPA1 mutations in amyotrophic lateral sclerosis;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2024-05-08

4. Conformational ensembles of the human intrinsically disordered proteome;Nature;2024-01-31

5. Nuclear-import receptors as gatekeepers of pathological phase transitions in ALS/FTD;Molecular Neurodegeneration;2024-01-22

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