Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/5/12/1953/1863788/5-12-1953.pdf
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1. Patterns of Clinical Progression Among Patients With Autosomal Recessive Limb-Girdle Muscular Dystrophy: A Systematic Review;Journal of Clinical Neuromuscular Disease;2023-12
2. Childhood muscular dystrophies;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023
3. Progression to Loss of Ambulation Among Patients with Autosomal Recessive Limb-girdle Muscular Dystrophy: A Systematic Review;Journal of Neuromuscular Diseases;2022-07-01
4. Advanced Gene-Targeting Therapies for Motor Neuron Diseases and Muscular Dystrophies;International Journal of Molecular Sciences;2022-04-27
5. Clinical Determinants of Disease Progression in Patients With Beta-Sarcoglycan Gene Mutations;Frontiers in Neurology;2021-07-01
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