732831

Source:http://linkedlifedata.com/resource/pubmed/id/732831

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019880, umls-concept:C0231330, umls-concept:C0268615, umls-concept:C0332307
pubmed:dateCreated	1979-3-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7600568
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Methylenetetrahydrofolate..., http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases
pubmed:status	MEDLINE
pubmed:issn	0077-0876
pubmed:author	pubmed-author:ArakawaTT, pubmed-author:NarisawaKK, pubmed-author:WadaYY
pubmed:issnType	Print
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	140-6
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:732831-Apnea, pubmed-meshheading:732831-Brain, pubmed-meshheading:732831-Consanguinity, pubmed-meshheading:732831-Female, pubmed-meshheading:732831-Genes, Recessive, pubmed-meshheading:732831-Heterozygote Detection, pubmed-meshheading:732831-Homocystinuria, pubmed-meshheading:732831-Homozygote, pubmed-meshheading:732831-Humans, pubmed-meshheading:732831-Infant, pubmed-meshheading:732831-Infant, Newborn, pubmed-meshheading:732831-Infant, Newborn, Diseases, pubmed-meshheading:732831-Intellectual Disability, pubmed-meshheading:732831-Kidney, pubmed-meshheading:732831-Leukocytes, pubmed-meshheading:732831-Liver, pubmed-meshheading:732831-Methylenetetrahydrofolate Dehydrogenase (NADP), pubmed-meshheading:732831-Oxidoreductases, pubmed-meshheading:732831-Seizures, pubmed-meshheading:732831-Syndrome
pubmed:year	1978
pubmed:articleTitle	Infantile type of homocystinuria with 5,10-methylenetetrahydrofolate reductase deficiency.
pubmed:publicationType	Journal Article, Case Reports