Activating and dominant inactivating c-KIT catalytic domain mutations in distinct clinical forms of human mastocytosis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 4, 1999, Pages 1609-1614

  Longley Jr , B Jack ^a,b   Metcalfe, Dean D ^c   Tharp, Michael ^d   Wang, Xiaomei ^a   Tyrrell, Lynda ^b   Lu, Shu Zhuang ^b   Heitjan, David ^e   Ma, Yongsheng ^a,b  

^a Coll Phys Surgs of Columbia Univ ^*  (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

^d RUSH UNIVERSITY MEDICAL CENTER   (United States)

^e Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMIC ACID; INTERLEUKIN 3 RECEPTOR; LYSINE; PHENYLALANINE; STEM CELL FACTOR RECEPTOR; TYROSINE; VALINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; ENZYME ACTIVE SITE; FAMILIAL DISEASE; HUMAN; HUMAN TISSUE; NEWBORN; PRIORITY JOURNAL; SOMATIC MUTATION; URTICARIA PIGMENTOSA;

ADULT; AMINO ACID SUBSTITUTION; ASPARTIC ACID; CATALYTIC DOMAIN; CHILD; CHILD, PRESCHOOL; HUMANS; INFANT; INFANT, NEWBORN; MASTOCYTOSIS; MIDDLE AGED; POINT MUTATION; PROTO-ONCOGENE PROTEINS C-KIT; VALINE;

EID: 13044305857     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.4.1609     Document Type: Article

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