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PMID: 11112388 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).

Blood cells, molecules & diseases ·Vol. 26 ·No. 5 ·2000-10-00 ·Pages 561-5

Cross AR, Noack D, Rae J, Curnutte JT, Heyworth PG

Abstract

暂无摘要

MeSH Terms

Child Genes, Recessive Granulomatous Disease, Chronic/genetics Humans Membrane Transport Proteins Mutation NADPH Dehydrogenase/genetics NADPH Oxidases Phosphoproteins/genetics

Chemicals

Membrane Transport Proteins Phosphoproteins neutrophil cytosol factor 67K NADPH Oxidases CYBA protein, human neutrophil cytosolic factor 1 NADPH Dehydrogenase

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Cross A R

Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

Noack D

Rae J

Curnutte J T

Heyworth P G

Article Info

Journal

Blood cells, molecules & diseases

Abbr.

Blood Cells Mol Dis

ISSN

1079-9796

DOI

10.1006/bcmd.2000.0333

Published

2000-10-00

Pages

561-5

Language

English

Region

United States

NLM ID

9509932

Subset

Grants

NIAID NIH HHS · AI24838 · United States

NCI NIH HHS · CA68276 · United States

External Links

PubMed source DOI: 10.1006/bcmd.2000.0333 View journal details

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Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).

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