A novel germline KIT mutation (p.L576P) in a family presenting with Juvenile onset of multiple gastrointestinal stromal tumors, skin hyperpigmentations, and esophageal stenosis
Teresa M. Neuhann, Veit Mansmann, Sabine Merkelbach-Bruse, Barbara Klink, Achim Hellinger, Heinz Gert Höffkes, Eva Wardelmann, Hans Ulrich Schildhaus, Sigrid Tinschert*
*Corresponding author for this work
Research output: Contribution to journal › Article › Research › peer-review
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