High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors

Intensive analysis of the SMARCB1 gene in malignant rhabdoid tumors (MRT) revealed eight of 16 patients with constitutional genetic variants. Three patients had mosaicism of deletion/variant of the SMARCB1 gene, which conventional methods might overlook. The prevalence of cancer predisposition in MR...

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Vydáno v:Eur J Hum Genet
Hlavní autoři: Shirai, Ryota, Osumi, Tomoo, Terashima, Keita, Kiyotani, Chikako, Uchiyama, Meri, Tsujimoto, Shinichi, Yoshida, Masanori, Yoshida, Kaoru, Uchiyama, Toru, Tomizawa, Daisuke, Shioda, Yoko, Sekiguchi, Masahiro, Watanabe, Kenichiro, Keino, Dai, Ueno-Yokohata, Hitomi, Ohki, Kentaro, Takita, Junko, Ito, Shuichi, Deguchi, Takao, Kiyokawa, Nobutaka, Ogiwara, Hideki, Hishiki, Tomoro, Ogawa, Seishi, Okita, Hajime, Matsumoto, Kimikazu, Yoshioka, Takako, Kato, Motohiro
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer International Publishing 2020
Témata:
Brief Communication
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7381660/
https://ncbi.nlm.nih.gov/pubmed/32218533
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-0614-z
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