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PMID: 7006308 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Acta paediatrica Scandinavica. Supplement ·Vol. 280 ·1980-00-00 ·Pages 1-80

Güttler F

Abstract

暂无摘要

MeSH Terms
Amino Acid Metabolism, Inborn Errors/classification,diagnosis,genetics Genetic Carrier Screening Humans Infant, Newborn Intellectual Disability/diagnosis,genetics Phenotype Phenylalanine/blood Phenylalanine Hydroxylase/deficiency Phenylketonurias/diagnosis,epidemiology,genetics Terminology as Topic
Chemicals
Phenylalanine Phenylalanine Hydroxylase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Güttler F
Article Info
Journal
Acta paediatrica Scandinavica. Supplement
Abbr.
Acta Paediatr Scand Suppl
ISSN
0300-8843
Published
1980-00-00
Pages
1-80
Language
English
Region
Sweden
NLM ID
0173166
Subset
IM
External Links
PubMed source
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