KIT Mutations and Other Genetic Defects in Mastocytosis

Key Findings

• ●Comprehensive review of KIT mutations and additional genetic defects in SM
• ●KIT D816V present in >90% of adult SM when sensitive assays used

Referenced in (1 disease)

1. passsource metadataJun 1, 2026, 04:40 PMby pubmed-api

   Stored DOI was incorrect; corrected to the PubMed-registered DOI (verified to resolve to this article).

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