Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India

Neurogenetics, Vol. 24, Issue 1, Pages 43-53, 2022

PMID: 36580222

Dysferlinopathies are a group of limb-girdle muscular dystrophies causing significant disability in the young population. There is a need for studies on large cohorts to describe the clinical, genotypic and natural history in our subcontinent. To describe and correlate the clinical, genetic profile and natural history of genetically confirmed dysferlinopathies.

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