Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population-Reference-Cited by-同舟云学术

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Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population

Published:1999-03-01 Issue:5 Volume:52 Page:1015-1015
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Chou F.-L.,Angelini C.,Daentl D.,Garcia C.,Greco C.,Hausmanowa-Petrusewicz I.,Fidzianska A.,Wessel H.,Hoffman E. P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 53 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. Diagnosis of Two Unrelated Syndromes of Prader-Willi and Calpainopathy: Insight from Trio Whole Genome Analysis and Isodisomy Mapping;Genes;2024-07-19

2. Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1;Orphanet Journal of Rare Diseases;2024-04-01

3. Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants;Molecular Genetics & Genomic Medicine;2022-11-14

4. Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India;Global Medical Genetics;2021-11-09

5. Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy Type 2A/R1 (LGMD2A/LGMDR1) Patients in India;Journal of Neuromuscular Diseases;2021-01-01

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