Novel R634W c-kit mutation identified in familial mastocytosis

Pediatric Dermatology

Volumn 32, Issue 2, 2015, Pages 267-270

  Pollard, Whitney L ^a   Beachkofsky, Thomas M ^b   Kobayashi, Todd T ^b  

^a SAN ANTONIO MILITARY MEDICAL CENTER   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; STEM CELL FACTOR RECEPTOR; TRYPTOPHAN;

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BLOOD SAMPLING; CASE REPORT; CELL INFILTRATION; CHILD; CHRONIC MYELOMONOCYTIC LEUKEMIA; DARIER DISEASE; FEMALE; FLUSHING; FOLLOW UP; GENETIC ANALYSIS; HUMAN; MALE; MAST CELL; MASTOCYTOMA; MASTOCYTOSIS; MELANOMA; MISSENSE MUTATION; MONOZYGOTIC TWINS; PAPULE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; PUNCH BIOPSY; SCRATCHING; SEQUENCE ANALYSIS; SIBLING; URTICARIA PIGMENTOSA; GENETIC PREDISPOSITION; GENETICS; IMMUNOHISTOCHEMISTRY; MASTOCYTOSIS, CUTANEOUS; MUTATION; NEEDLE BIOPSY; PEDIGREE; PHYSIOLOGIC MONITORING; PROGNOSIS; RISK ASSESSMENT;

BIOPSY, NEEDLE; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MASTOCYTOSIS, CUTANEOUS; MONITORING, PHYSIOLOGIC; MUTATION; PEDIGREE; PROGNOSIS; PROTO-ONCOGENE PROTEINS C-KIT; RISK ASSESSMENT; SIBLINGS; URTICARIA PIGMENTOSA;

EID: 84925297318     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/pde.12381     Document Type: Article

References (15)

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