Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1989-5-10
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0066-4197
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
22
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
301-21
|
pubmed:dateRevised |
2005-11-17
|
pubmed:meshHeading |
pubmed-meshheading:3071251-Amino Acid Metabolism, Inborn Errors,
pubmed-meshheading:3071251-Dihydropteridine Reductase,
pubmed-meshheading:3071251-Genes,
pubmed-meshheading:3071251-Humans,
pubmed-meshheading:3071251-Phenylalanine,
pubmed-meshheading:3071251-Phenylalanine Hydroxylase,
pubmed-meshheading:3071251-Phenylketonurias
|
pubmed:year |
1988
|
pubmed:articleTitle |
Mendelian hyperphenylalaninemia.
|
pubmed:affiliation |
Centre for Human Genetics, McGill University, Montreal, Quebec, Canada.
|
pubmed:publicationType |
Journal Article,
Review
|