Renal angiomyolipoma (AML) harboring a missense mutation of TSC2 with copy-neutral loss of heterozygosity (CN-LOH)

Angiomyolipoma (AML) is classified as a perivascular epithelioid cell neoplasm, mostly occurring in the kidney. Twenty percent of patients with renal AML have tuberous sclerosis complex (TSC) caused by germline variation in the TSC1 or TSC2 gene. In this paper, we report the first case of renal AML...

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Detalles Bibliográficos
Publicado en:Cancer Biol Ther
Main Authors: Idogawa, Masashi, Hida, Tokimasa, Tanaka, Toshiaki, Ohira, Noriaki, Tange, Shoichiro, Sasaki, Yasushi, Uhara, Hisashi, Masumori, Naoya, Tokino, Takashi, Natori, Hiroshi
Formato: Artigo
Idioma:Inglês
Publicado: Taylor & Francis 2019
Assuntos:
Bedside-to-Bench Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7515489/
https://ncbi.nlm.nih.gov/pubmed/31847710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384047.2019.1702406
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