A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy

Anju Shukla, Dhanya L. Narayanan, Urja Asher, Katta M. Girisha

Research output: Contribution to journalLetterpeer-review

5 Citations (Scopus)
Original languageEnglish
Pages (from-to)276-277
Number of pages2
JournalClinical Genetics
Issue number3
Publication statusPublished - 01-01-2019

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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