טוען...
Novel missense mutation in the FH gene in familial renal cell cancer patients lacking cutaneous leiomyomas
BACKGROUND: Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare tumor predisposition syndrome characterized by cutaneous and uterine leiomyomas and papillary type 2 renal cell cancer. Germline mutation of the fumarate hydratase (FH) gene is known to be associated with HLRCC. CASE PRESE...
שמור ב:
| Main Authors: | , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3978052/ https://ncbi.nlm.nih.gov/pubmed/24684806 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-7-203 |
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