Spectrum of hypermethioninemia in neonatal screening

Early Human Development

Volumn 81, Issue 6, 2005, Pages 529-533

  Chien, Yin Hsiu ^a   Chiang, Shu Chuan ^a   Huang, Aichu ^a   Hwu, Wuh Liang ^a  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

Chinese; Homocystinuria; Isolated hypermethioninemia; Methionine adenosyltransferase deficiency; Neonatal screening; Taiwan

Indexed keywords

METHIONINE ADENOSYLTRANSFERASE;

AMINO ACID BLOOD LEVEL; ARTICLE; CLINICAL ARTICLE; DIET; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; ENZYME DEFICIENCY; FEMALE; FOLLOW UP; GENE IDENTIFICATION; GENE MUTATION; HEALTH PROGRAM; HOMOCYSTINURIA; HUMAN; HYPERMETHIONINEMIA; INTELLIGENCE QUOTIENT; MALE; MEASUREMENT; NEWBORN; NEWBORN SCREENING; PREVALENCE;

AMINO ACID METABOLISM, INBORN ERRORS; DIAGNOSIS, DIFFERENTIAL; FEMALE; HOMOCYSTINURIA; HUMANS; INFANT, NEWBORN; METHIONINE; METHIONINE ADENOSYLTRANSFERASE; NEONATAL SCREENING; PREVALENCE; TREATMENT OUTCOME;

EID: 20344371231     PISSN: 03783782     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.earlhumdev.2004.11.005     Document Type: Article

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