Congenital bullous mastocytosis with myeloproliferative disorder and c- kit mutation

Journal of the American Academy of Dermatology

Volumn 39, Issue 1, 1998, Pages 119-121

  Shah, P Y ^a   Sharma, V ^a   Worobec, A S ^a   Metcalfe, D D ^a   Zwick, D C ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

STEM CELL FACTOR;

ARTICLE; BULLOUS SKIN DISEASE; CASE REPORT; CELL PROLIFERATION; GENE MUTATION; HUMAN; INFANT; MALE; MASTOCYTOSIS; MONONUCLEAR CELL; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; PROGNOSIS;

EID: 0031851296     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0190-9622(98)70413-X     Document Type: Article

References (10)

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6. H Nagata AS Worobec CK Oh BA Chowdhury S Tannenbaum Y Suzuki Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder Proc Natl Acad Sci U S A 92 1995 10560 10564
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