Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies-Reference-Cited by-同舟云学术

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Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies

Published:2017-02-03 Issue:1 Volume:56 Page:117-121
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Zhong Jingzi¹,Xu Tiantian¹,Chen Gang²,Liao Haixia¹,Zhang Jiapeng¹,Lan Dan¹³

Affiliation:

1. Department of Pediatrics; The First Affiliated Hospital of Guangxi Medical University; China

2. Department of Pathology; The First Affiliated Hospital of Guangxi Medical University; China

3. Team for Major Disease Prevention and Control; The First Affiliated Hospital of Guangxi Medical University; China

Funder

the First Affiliated Hospital of Guangxi Medical University starting fund for study abroad returnees

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.25435/fullpdf

Reference20 articles.

1. Population frequencies of inherited neuromuscular diseases--a world survey;Emery;Neuromuscul Disord,1991

2. The muscular dystrophies;Emery;Lancet,2002

3. Emerging genetic therapies to treat Duchenne muscular dystrophy;Nelson;Curr Opin Neurol,2009

4. Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches;Fairclough;Nat Rev Genet,2013

5. Deletion and duplication screening in the DMD gene using MLPA;Lalic;Eur J Hum Genet,2005

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1. Clinical Diagnosis and Genetic Analysis of Children With Muscular Dystrophies;Clinical Pediatrics;2024-08-28

2. Identification of a Novel de novo Splicing Mutation in Duchenne Muscular Dystrophy Gene in an Iranian Family;Molecular Syndromology;2023

3. Duchenne Muscular Dystrophy With Low Acidic α-Glucosidase Activity: Two Case Reports and Literature Review;Frontiers in Pediatrics;2022-06-01

4. Clinical Diagnosis and Genetic Analysis of Children with Muscular Dystrophies;SSRN Electronic Journal;2022

5. Application whole exome sequencing for the clinical molecular diagnosis of patients with Duchenne muscular dystrophy; identification of four novel nonsense mutations in four unrelated Chinese DMD patients;Molecular Genetics & Genomic Medicine;2019-04

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