Article
A distinct subset of atypical Spitz tumors is characterized by BRAF mutation and loss of BAP1 expression.
The American journal of surgical pathology - 1 Jun 2012
Wiesner Thomas, Murali Rajmohan, Fried Isabella, Cerroni Lorenzo, Busam Klaus, Kutzner Heinz, Bastian Boris C
Abstract excerpt
We recently reported that germline mutations in BAP1 cause a familial tumor syndrome characterized by high penetrance for melanocytic tumors with distinct clinical and histologic features. Melanocytic neoplasms in affected individuals harbored BRAF mutations, showed loss of BAP1 expression, and h...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
