Metabolic heritability at birth: Implications for chronic disease research

Human Genetics

Volumn 133, Issue 8, 2014, Pages 1049-1057

  Ryckman, Kelli K ^a   Smith, Caitlin J ^a   Jelliffe Pawlowski, Laura L ^b,c   Momany, Allison M ^d   Berberich, Stanton L ^e   Murray, Jeffrey C ^d  

^a UNIVERSITY OF IOWA   (United States)

^b Genetic Disease Screening Program California Department of Public Health   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF IOWA   (United States)

^e UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASES; ADULT; CARNITINE; CHRONIC DISEASE; FEMALE; HUMANS; INFANT, NEWBORN; LIPID METABOLISM, INBORN ERRORS; MALE; METABOLISM, INBORN ERRORS; ORGANIC CATION TRANSPORT PROTEINS; TANDEM MASS SPECTROMETRY;

EID: 84904426498     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-014-1450-4     Document Type: Article

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