Molecular Basis of Congenital Neutropenia

Overview

Journal Haematologica

Specialty Hematology

Date 2009 Oct 2

PMID 19794077

Citations 4

Authors

Christoph Klein

Affiliations

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Citing Articles

Serpin B1 defect and increased apoptosis of neutrophils in Cohen syndrome neutropenia.

Duplomb L, Riviere J, Jego G, Da Costa R, Hammann A, Racine J J Mol Med (Berl). 2019; 97(5):633-645.

PMID: 30843084 DOI: 10.1007/s00109-019-01754-4.

A novel compound heterozygous HAX1 mutation in a Chinese patient with severe congenital neutropenia and chronic myelomonocytic leukemia transformation but without neurodevelopmental abnormalities.

Xue S, Li J, Zou J, Su J, Chen S, Wu D Haematologica. 2011; 97(2):318-20.

PMID: 22102707 PMC: 3269495. DOI: 10.3324/haematol.2011.055038.

Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3.

Banka S, Chervinsky E, Newman W, Crow Y, Yeganeh S, Yacobovich J Eur J Hum Genet. 2010; 19(1):18-22.

PMID: 20717171 PMC: 3039503. DOI: 10.1038/ejhg.2010.136.

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia.

Lanciotti M, Indaco S, Bonanomi S, Coliva T, Mastrodicasa E, Caridi G Haematologica. 2010; 95(1):168-9.

PMID: 20065084 PMC: 2805731. DOI: 10.3324/haematol.2009.015370.

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