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PMID: 2425263 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location.

Nature ·Vol. 322 ·No. 6074 ·1986-00-00 ·Pages 32-8

Royer-Pokora B, Kunkel LM, Monaco AP, Goff SC, Newburger PE, Baehner RL, Cole FS, Curnutte JT, Orkin SH

Abstract

The gene that is abnormal in the X-linked form of the phagocytic disorder chronic granulomatous disease has been cloned without reference to a specific protein by relying on its chromosomal map position. The transcript of the gene is expressed in the phagocytic lineage of haematopoietic cells and is absent or structurally abnormal in four patients with the disorder. The nucleotide sequence of complementary DNA clones predicts a polypeptide of at least 468 amino acids with no homology to proteins described previously.

MeSH Terms
Amino Acid Sequence Base Sequence Chromosome Deletion Chromosome Mapping Cloning, Molecular DNA/analysis Gene Expression Regulation Granulomatous Disease, Chronic/genetics Humans Leukemia, Myeloid, Acute/genetics RNA/analysis Tissue Distribution Transcription, Genetic
Chemicals
RNA DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Royer-Pokora B
Kunkel L M
Monaco A P
Goff S C
Newburger P E
Baehner R L
Cole F S
Curnutte J T
Orkin S H
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1986-00-00
Pages
32-8
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NIAID NIH HHS · AI-21320 · United States
NCI NIH HHS · CA38325 · United States
NICHD NIH HHS · HD18661 · United States
Databases
GENBANK
X04011
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