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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