Rare variant in the fumarate hydratase gene found in patients with clinical features of hereditary leiomyomatosis and renal cell cancer (HLRCC): A case series.
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| Title: | Rare variant in the fumarate hydratase gene found in patients with clinical features of hereditary leiomyomatosis and renal cell cancer (HLRCC): A case series. |
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| Authors: | Franke K; Master of Genetic Counselor Studies Program, Department of Pediatrics University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA.; Present address: Department of Molecular and Medical Genetics Oregon Health & Science University Portland Oregon USA., Vagher J; Huntsman Cancer Institute at the University of Utah Salt Lake City Utah USA., Boyle J; Huntsman Cancer Institute at the University of Utah Salt Lake City Utah USA., Hall A; Master of Genetic Counselor Studies Program, Department of Pediatrics University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA.; Center for Human Genomics and Precision Medicine University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA., Smith-Simmer K; Master of Genetic Counselor Studies Program, Department of Pediatrics University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA.; Oncology Genetics, University of Wisconsin Carbone Cancer Center UW Health Madison Wisconsin USA. |
| Source: | Clinical case reports [Clin Case Rep] 2022 Mar 01; Vol. 10 (3), pp. e05513. Date of Electronic Publication: 2022 Mar 01 (Print Publication: 2022). |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101620385 Publication Model: eCollection Cited Medium: Print ISSN: 2050-0904 (Print) Linking ISSN: 20500904 NLM ISO Abbreviation: Clin Case Rep Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2050-0904 |
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| DOI: | 10.1002/ccr3.5513 |
