Resources

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.

Read More

  https://www.ncbi.nlm.nih.gov/pubmed/36580222

 

Considering Genomic Research?

    Fields marked in * is mandatory to fill

     

     


     


    2023 © MedGenome • All Rights Reserved
    Request a Quote