Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Any myopathy in which the cause of the disease is a variation in the POMGNT1 gene.
No clinical trials have been registered for myopathy caused by variation in POMGNT1.
6 publications have been identified in PubMed for myopathy caused by variation in POMGNT1. Research spans Basic Science / Preclinical (33%), Epidemiology / Natural History (33%), and Review / Meta-Analysis (17%).
Flannery KP (2026). [PMID: 41533692](https://pubmed.ncbi.nlm.nih.gov/41533692/). *PLoS genetics*. [Basic Science / Preclinical]
Cicala G (2026). [PMID: 41836883](https://pubmed.ncbi.nlm.nih.gov/41836883/). *Neurology. Genetics*. [Epidemiology / Natural History]
Ziccardi L (2025). [PMID: 40244109](https://pubmed.ncbi.nlm.nih.gov/40244109/). *International journal of molecular sciences*. [Case Report / Case Series]
Khalilian S (2025). [PMID: 40361203](https://pubmed.ncbi.nlm.nih.gov/40361203/). *Human genomics*. [Epidemiology / Natural History]
Mohan S (2024). [PMID: 39215466](https://pubmed.ncbi.nlm.nih.gov/39215466/). *Annals of clinical and translational neurology*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:58 PM UTC
Mohan S (2024). [PMID: 38765987](https://pubmed.ncbi.nlm.nih.gov/38765987/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]