Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy-Reference-Cited by-同舟云学术

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Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy

Published:2007-02-27 Issue:6 Volume:44 Page:368-372
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Taylor P. J,Maroulis S.,Mullan G. L,Pedersen R. L,Baumli A.,Elakis G.,Piras S.,Walsh C.,Prosper-Gutierrez B.,De La Puente-Alonso F.,Bell C. G,Mowat D. R,Johnston H. M,Buckley M. F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 42 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. The complex landscape of DMD mutations: moving towards personalized medicine;Frontiers in Genetics;2024-03-26

2. Clinical spectrum of manifestations in symptomatic female with Duchenne muscular dystrophy: A concise review;Translational Science of Rare Diseases;2023-09-30

3. Sex differences in neuromuscular disorders;Mechanisms of Ageing and Development;2023-04

4. The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies;Vojnosanitetski pregled;2023

5. Factors associated with balance ability in Duchenne and Becker muscular dystrophies;Gait & Posture;2023-01

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