Resources

Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Journal of clinical neurology (Seoul, Korea), Vol. 17, Issue 3, Pages 409-418, 2021

PMID: 34184449

Pathogenic variants in the myopalladin gene (MYPN) are known to cause mildly progressive nemaline/cap myopathy. Only nine cases have been reported in the English literature.

Read More

  https://www.ncbi.nlm.nih.gov/pubmed/34184449

 

Considering Genomic Research?

    Fields marked in * is mandatory to fill
     
     
     

    2024 © MedGenome • All Rights Reserved
    Request a Quote