7006308

Source:http://linkedlifedata.com/resource/pubmed/id/7006308

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008902, umls-concept:C0011900, umls-concept:C0231335, umls-concept:C0332307, umls-concept:C0751434, umls-concept:C0751435
pubmed:dateCreated	1981-3-17
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0173166
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine, http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine Hydroxylase
pubmed:status	MEDLINE
pubmed:issn	0300-8843
pubmed:author	pubmed-author:GüttlerFF
pubmed:issnType	Print
pubmed:volume	280
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1-80
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:7006308-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:7006308-Heterozygote Detection, pubmed-meshheading:7006308-Humans, pubmed-meshheading:7006308-Infant, Newborn, pubmed-meshheading:7006308-Intellectual Disability, pubmed-meshheading:7006308-Phenotype, pubmed-meshheading:7006308-Phenylalanine, pubmed-meshheading:7006308-Phenylalanine Hydroxylase, pubmed-meshheading:7006308-Phenylketonurias, pubmed-meshheading:7006308-Terminology as Topic
pubmed:year	1980
pubmed:articleTitle	Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.
pubmed:publicationType	Journal Article, Review, Research Support, Non-U.S. Gov't