Mutations in SDHC cause autosomal dominant paraganglioma, type 3
- PMID: 11062460
- DOI: 10.1038/81551
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
Abstract
Nonchromaffin paragangliomas (PGLs) are usually benign, neural-crest-derived, slow-growing tumours of parasympathetic ganglia. Between 10% and 50% of cases are familial and are transmitted as autosomal dominant traits with incomplete and age-dependent penetrance.
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