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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for symptomatic form of X-linked centronuclear myopathy in female carriers.
3 publications have been identified in PubMed for symptomatic form of X-linked centronuclear myopathy in female carriers. Research spans Basic Science / Preclinical (67%) and Epidemiology / Natural History (33%).
Bohill J (2026). [PMID: 41806468](https://pubmed.ncbi.nlm.nih.gov/41806468/). *Neuromuscul Disord*. [Epidemiology / Natural History]
Mohar NP (2024). [PMID: 38732148](https://pubmed.ncbi.nlm.nih.gov/38732148/). *Int J Mol Sci*. [Basic Science / Preclinical]
de Feraudy Y (2024). [PMID: 38982518](https://pubmed.ncbi.nlm.nih.gov/38982518/). *Genome Med*. [Basic Science / Preclinical]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:41 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center