C-kit activating mutation in a neonate with in-utero presentation of systemic mastocytosis associated with myeloproliferative disorder [6]

British Journal of Haematology

Volumn 106, Issue 3, 1999, Pages 838-839

  Kuint, J ^a   Bielorai, K J ^a   Gilat, B ^a   Birenbaum, D ^a   Amariglio, E ^a   Rechavi, N G ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

Activating mutation; C kit; Mastocytosis; Myeloproliferative disorder; Stem cell factor

Indexed keywords

STEM CELL FACTOR;

CASE REPORT; DISEASE ASSOCIATION; GENE MUTATION; HEPATOSPLENOMEGALY; HUMAN; INFANT; LETTER; MALE; MASTOCYTOSIS; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; PROTO ONCOGENE;

HUMANS; INFANT; MALE; MASTOCYTOSIS; MUTATION; MYELOPROLIFERATIVE DISORDERS; PROTO-ONCOGENE PROTEINS C-KIT;

EID: 0032827839     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1999.01683.x     Document Type: Letter

References (7)