Novel Germline Mutation of KIT Associated With Familial Gastrointestinal Stromal Tumors and Mastocytosis-Reference-Cited by-同舟云学术

Novel Germline Mutation of KIT Associated With Familial Gastrointestinal Stromal Tumors and Mastocytosis

Published:2005-09 Issue:3 Volume:129 Page:1042-1046
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Hartmann Karin,Wardelmann Eva,Ma Yongsheng,Merkelbach–Bruse Sabine,Preussner Liane M.,Woolery Carla,Baldus Stephan E.,Heinicke Thomas,Thiele Juergen,Buettner Reinhard,Longley B. Jack

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference27 articles.

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3. Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis;Longley;Nat Genet,1996

4. Activating and dominant inactivating c-KIT catalytic domain mutations in distinct clinical forms of human mastocytosis;Longley;Proc Natl Acad Sci U S A,1999

5. Achalasia due to diffuse esophageal leiomyomatosis and inherited as an autosomal dominant disorder. Report of a family study;Marshall;Gastroenterology,1990

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