Phenotypic Heterogeneity of Neutropenia and Gastrointestinal Illness Associated with G6PC3 Founder Mutation-Reference-Cited by-同舟云学术

Phenotypic Heterogeneity of Neutropenia and Gastrointestinal Illness Associated with G6PC3 Founder Mutation

Published:2016-10 Issue:7 Volume:38 Page:e243-e247
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Glasser Chana L.,Picoraro Joseph A.,Jain Preti,Kinberg Sivan,Rustia Evelyn,Gross Margolis Kara,Anyane-Yeboa Kwame,Iglesias Alejandro D.,Green Nancy S.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference20 articles.

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2. A syndrome with congenital neutropenia and mutations in G6PC3;Boztug;N Engl J Med,2009

3. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis;Horwitz;Nat Genet,1999

4. Genetics and pathophysiology of severe congenital neutropenia syndromes unrelated to neutrophil elastase;Boztug;Hematol Oncol Clin North Am,2013

5. A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations;Banka;Orphanet J Rare Dis,2013

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