| Literature DB >> 17908262 |
W Heinritz1, U Paasch, M Sticherling, C Wittekind, J C Simon, U G Froster, R Renner.
Abstract
We report on the results of clinical investigation, pedigree analysis, mutation screening and haplotyping in a family with the syndrome of multiple cutaneous and uterine leiomyomas (MCUL1) and a germline missense mutation (R58P) in the fumarate hydratase gene (FH). We provide evidence for a founder effect for the identified mutation and distant relationship of our family to another familial case of MCUL1 associated with renal cell cancer, which was recently published with the same mutation.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17908262 DOI: 10.1111/j.1469-1809.2007.00396.x
Source DB: PubMed Journal: Ann Hum Genet ISSN: 0003-4800 Impact factor: 1.670