Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis-Reference-Cited by-同舟云学术

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Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis

Published:2018-05-22 Issue: Volume:12 Page:
ISSN:1662-453X
Container-title:Frontiers in Neuroscience
language:
Short-container-title:Front. Neurosci.

Author:

Lu Yan,Da Yu-Wei,Zhang Yong-Biao,Li Xin-Gang,Wang Min,Di Li,Pang Mi,Lei Lin

Publisher

Frontiers Media SA

Subject

General Neuroscience

Reference27 articles.

1. “Rimmed vacuole myopathy” sparing the quadriceps. A unique disorder in Iranian Jews;Argov;J. Neurol. Sci.,1984

2. New advances in inclusion-body myositis;Askanas;Curr. Opin. Rheumatol.,1993

3. Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis;Askanas;Curr. Opin. Rheumatol.,1998

4. Hereditary inclusion-body myopathies;Broccolini;Biochim. Biophys. Acta,2015

5. Cloning of the human interferon-related developmental regulator (IFRD1) gene coding for the PC4 protein, a member of a novel family of developmentally regulated genes;Buanne;Genomics,1998

Cited by 2 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. Heterozygous Cystic Fibrosis Transmembrane Regulator Gene Missense Variants Are Associated With Worse Cardiac Function in Patients With Duchenne Muscular Dystrophy;Journal of the American Heart Association;2020-10-06

2. Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis;Frontiers in Neuroscience;2018-08-22

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