Prevalence of c-KIT Mutations in Gonadoblastoma and Dysgerminomas of Patients with Disorders of Sex Development (DSD) and Ovarian Dysgerminomas

Activating c-KIT mutations (exons 11 and 17) are found in 10–40% of testicular seminomas, the majority being missense point mutations (codon 816). Malignant ovarian dysgerminomas represent ∼3% of all ovarian cancers in Western countries, resembling testicular seminomas, regarding chromosomal aberrat...

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Hlavní autoři: Hersmus, Remko, Stoop, Hans, van de Geijn, Gert Jan, Eini, Ronak, Biermann, Katharina, Oosterhuis, J. Wolter, DHooge, Catharina, Schneider, Dominik T., Meijssen, Isabelle C., Dinjens, Winand N. M., Dubbink, Hendrikus Jan, Drop, Stenvert L. S., Looijenga, Leendert H. J.
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2012
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3429439/
https://ncbi.nlm.nih.gov/pubmed/22937135
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0043952
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