MYOD1

Publications

Ashton C et al. Expanding the MYOD1 Phenotype: A Case Report of a Patient Diagnosed Whilst Pregnant. J Neuromuscul Dis. 2022;9(5):615-618. PMID: 35754284.

Lopes F et al. MYOD1 involvement in myopathy. Eur J Neurol. 2018;25(12):e123-e124. PMID: 30403323.

Shukla A et al. A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy. Clin Genet. 2019;96(3):276-277. PMID: 31260566.

Watson CM et al. Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia. J Med Genet. 2016;53(4):264-9. PMID: 26733463.