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Any myopathy in which the cause of the disease is a variation in the CRPPA gene.
Biomarker and diagnostic research for myopathy caused by variation in CRPPA has been reported in the published literature.
No clinical trials have been registered for myopathy caused by variation in CRPPA.
4 publications have been identified in PubMed for myopathy caused by variation in CRPPA. Research spans Diagnostic / Biomarker (25%), Review / Meta-Analysis (25%), and Basic Science / Preclinical (25%).
Rahmuni Y (2026). [PMID: 41742649](https://pubmed.ncbi.nlm.nih.gov/41742649/). *Molecular genetics & genomic medicine*. [Diagnostic / Biomarker]
Germain A (2025). [PMID: 41237904](https://pubmed.ncbi.nlm.nih.gov/41237904/). *Molecular & cellular proteomics : MCP*. [Basic Science / Preclinical]
Kim SH (2025). [PMID: 40390582](https://pubmed.ncbi.nlm.nih.gov/40390582/). *Journal of Korean medical science*. [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, 5:37 AM UTC