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Updated: Jul 16, 2026

Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
[From gene to disease; cutaneous leiomyomatosis]
S Badeloe1, M van Geel, M A M van Steensel
1Afd. Dermatologie, Academisch Ziekenhuis Maastricht, Postbus 5800, 6202 AZ Maastricht. sbad@sder.azm.nl
Abstract:
Multiple cutaneous and uterine leiomyomatosis (MCUL; OMIM 150800) is an autosomal dominantly inherited disease characterized by leiomyomas of the skin and uterine leiomyomas. MCUL can be associated with various types of renal cancer. This syndrome is known as hereditary leiomyomatosis and renal cell cancer (HLRCC; OMIM 605839). Both disorders result from heterozygous germline mutations in the fumarate hydratase (FH) gene.
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