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Any myopathy in which the cause of the disease is a variation in the POMT2 gene.
No clinical trials have been registered for myopathy caused by variation in POMT2.
3 publications have been identified in PubMed for myopathy caused by variation in POMT2. Research spans Review / Meta-Analysis (33%), Basic Science / Preclinical (33%), and Epidemiology / Natural History (33%).
Yang G (2025). [PMID: 40102912](https://pubmed.ncbi.nlm.nih.gov/40102912/). *Orphanet J Rare Dis*. [Basic Science / Preclinical]
Kale MY (2025). [PMID: 40774080](https://pubmed.ncbi.nlm.nih.gov/40774080/). *Eur J Paediatr Neurol*. [Epidemiology / Natural History]
Mohan S (2024). [PMID: 39215466](https://pubmed.ncbi.nlm.nih.gov/39215466/). *Ann Clin Transl Neurol*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 1:11 PM UTC