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PMID: 2744764 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease.

Genomics ·Vol. 4 ·No. 4 ·1989-05-00 ·Pages 552-9

Lan NC, Heinzmann C, Gal A, Klisak I, Orth U, Lai E, Grimsby J, Sparkes RS, Mohandas T, Shih JC

Abstract

Monoamine oxidase A and B (MAO A and B) are the central enzymes that catalyze oxidative deamination of biogenic amines throughout the body. The regional locations of genes encoding MAO A and B on the X chromosome were determined by using full-length cDNA clones for human MAO A and B, respectively. Using somatic cell hybrids, in situ hybridization, and field-inversion gel electrophoresis as well as deletion mapping in a patient with Norrie disease, we concluded that these two genes are close to each other and to the DXS7 locus (Xp 11.3).

MeSH Terms
Animals Blindness/enzymology,genetics Chromosome Deletion Chromosome Mapping DNA/genetics Humans Hybrid Cells Male Mice Monoamine Oxidase/genetics Restriction Mapping Retina/abnormalities X Chromosome
Chemicals
DNA Monoamine Oxidase
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Lan N C
Division of Biological Sciences, School of Pharmacy, University of Southern California, Los Angeles 90033.
Heinzmann C
Gal A
Klisak I
Orth U
Lai E
Grimsby J
Sparkes R S
Mohandas T
Shih J C
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1989-05-00
Pages
552-9
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIMH NIH HHS · MH 37020 · United States
NIMH NIH HHS · MH 39085 · United States
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