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PMID: 4681915 Published · ppublish English Journal Article

Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.

The New England journal of medicine ·Vol. 288 ·No. 1 ·1973-01-04 ·Pages 7-12

Short EM, Conn HO, Snodgrass PJ, Campbell AG, Rosenberg LE

Abstract

暂无摘要

MeSH Terms
Adult Amino Acid Metabolism, Inborn Errors/diagnosis,genetics,therapy Ammonia/blood Biopsy, Needle Diet Therapy Dietary Proteins Female Genes, Dominant Heterozygote Humans Infant, Newborn Infant, Newborn, Diseases/diagnosis Liver/enzymology Male Mutation Ornithine Carbamoyltransferase/metabolism Pedigree Sex Chromosomes Sex Factors
Chemicals
Dietary Proteins Ammonia Ornithine Carbamoyltransferase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Short E M
Conn H O
Snodgrass P J
Campbell A G
Rosenberg L E
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1973-01-04
Pages
7-12
Language
English
Region
United States
NLM ID
0255562
Subset
IM
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