Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy-Reference-Cited by-同舟云学术

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Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy

Published:2014 Issue:6 Volume:62 Page:635
ISSN:0028-3886
Container-title:Neurology India
language:en
Short-container-title:Neurol India

Author:

Krahn Martin,Beroud Christophe,Xi Jianying,Blandin Gaelle,Lu Jiahong,Luo Sushan,Zhu Wenhua,Pecheux Christophe,Labelle Veronique,Levy Nicolas,Urtizberea JonAndoni,Zhao Chongbo

Publisher

Medknow

Subject

Clinical Neurology,Neurology

Cited by 25 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 Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments;Biomolecules;2024-02-21

2. Patterns of Clinical Progression Among Patients With Autosomal Recessive Limb-Girdle Muscular Dystrophy: A Systematic Review;Journal of Clinical Neuromuscular Disease;2023-12

3. Dysferlinopathy in Tunisia: clinical spectrum, genetic background and prognostic profile;Neuromuscular Disorders;2023-10

4. Genotype–phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India;neurogenetics;2022-12-29

5. Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case;Neuromuscular Diseases;2022-12-13

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