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Functional studies of a novel germline p53 splicing mutation identified in a patient with Li–Fraumeni-like syndrome

✍ Scribed by Jinhua Piao; Naoto Sakurai; Shotaro Iwamoto; Junji Nishioka; Kaname Nakatani; Yoshihiro Komada; Shuki Mizutani; Masatoshi Takagi

Book ID: 112142422
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 279 KB
Volume: aop
Category: Article
ISSN: 0899-1987
DOI: 10.1002/mc.21912

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## Abstract Germline __TP53__ mutations are found in Li‐Fraumeni syndrome (LFS) patients, predisposed to soft tissue sarcoma and other malignancies. The mutations and succeeding genetic events are thought to cause LFS‐associated cancer, whose genetic alterations have rarely been investigated. Here,