3329492

Source:http://linkedlifedata.com/resource/pubmed/id/3329492

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008902, umls-concept:C0019409, umls-concept:C0208973, umls-concept:C0751434, umls-concept:C0751435, umls-concept:C1517892, umls-concept:C1704666
pubmed:dateCreated	1988-5-31
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372421
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	0003-9764
pubmed:author	pubmed-author:LyonnetSS, pubmed-author:MunnichAA, pubmed-author:ReyFF, pubmed-author:ReyJJ
pubmed:issnType	Print
pubmed:volume	44 Suppl 1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	639-42
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:3329492-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:3329492-Child, pubmed-meshheading:3329492-Genetic Variation, pubmed-meshheading:3329492-Humans, pubmed-meshheading:3329492-Hydroxylation, pubmed-meshheading:3329492-Mutation, pubmed-meshheading:3329492-Phenylalanine, pubmed-meshheading:3329492-Phenylalanine Hydroxylase, pubmed-meshheading:3329492-Phenylketonurias
pubmed:year	1987
pubmed:articleTitle	[Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency].
pubmed:affiliation	Département de Pédiatrie, l'Unité de Recherche de Génétique Médicale (INSERM U12), Hôpital des Enfants Malades, Paris.
pubmed:publicationType	Journal Article, Review