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PMID: 14324515 Published · ppublish English Journal Article

HARTNUP DISEASE: A GENETIC MODIFICATION OF INTESTINAL AND RENAL TRANSPORT OF CERTAIN NEUTRAL ALPHA-AMINO ACIDS.

The New England journal of medicine ·Vol. 273 ·1965-09-02 ·Pages 530-2

SCRIVER CR

Abstract

暂无摘要

Keywords
AMINO ACID METABOLISM INBORN ERRORS AMINOACIDURIA RENAL CHROMATOGRAPHY ELECTROPHORESIS FECES HARTNUP DISEASE MALABSORPTION SYNDROMES RENAL TUBULAR TRANSPORT INBORN ERRORS URINE
MeSH Terms
Amino Acid Metabolism, Inborn Errors Amino Acids, Neutral Chromatography Electrophoresis Feces Hartnup Disease Humans Kidney Malabsorption Syndromes Renal Aminoacidurias Renal Tubular Transport, Inborn Errors Urine
Chemicals
Amino Acids, Neutral
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
SCRIVER C R
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
DOI
10.1056/NEJM196509022731005
Published
1965-09-02
Pages
530-2
Language
English
Region
United States
NLM ID
0255562
Subset
OM
External Links
PubMed source DOI: 10.1056/NEJM196509022731005 View journal details
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