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Any myopathy in which the cause of the disease is a variation in the POMT1 gene.
No clinical trials have been registered for myopathy caused by variation in POMT1.
5 publications have been identified in PubMed for myopathy caused by variation in POMT1. Research spans Review / Meta-Analysis (40%), Case Report / Case Series (20%), and Basic Science / Preclinical (20%).
Aleem T (2025). [PMID: 40730687](https://pubmed.ncbi.nlm.nih.gov/40730687/). *Eur J Hum Genet*. [Epidemiology / Natural History]
Quaio CRDC (2025). [PMID: 40360003](https://pubmed.ncbi.nlm.nih.gov/40360003/). *Arq Neuropsiquiatr*. [Review / Meta-Analysis]
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*. [Case Report / Case Series]
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, 4:32 PM UTC