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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Biochemistry, Genetics and Molecular Biology

Medicine and Dentistry