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A Novel Kindred with Familial Gastrointestinal Stromal Tumors Caused by a Rare KIT Germline Mutation (N655K): Clinico-Pathological Presentation and TKI Sensitivity
 
 
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J. Pers. Med. 2020, 10(4), 235; https://doi.org/10.3390/jpm10040235
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