20306460

Source:http://linkedlifedata.com/resource/pubmed/id/20306460

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0033053, umls-concept:C0152035, umls-concept:C0598429, umls-concept:C0751602, umls-concept:C1314792, umls-concept:C1412113, umls-concept:C2675528
pubmed:issue	5
pubmed:dateCreated	2010-5-4
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8106540
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SLC33A1 protein, human
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1097-0223
pubmed:author	pubmed-author:GadN MNM, pubmed-author:GongYaoqinY, pubmed-author:LinPengfeiP, pubmed-author:SekoYY, pubmed-author:ShaoChangshunC, pubmed-author:YanChuanzhuC
pubmed:issnType	Electronic
pubmed:volume	30
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	485-6
pubmed:meshHeading	pubmed-meshheading:20306460-Adult, pubmed-meshheading:20306460-Amniocentesis, pubmed-meshheading:20306460-China, pubmed-meshheading:20306460-Chromosome Mapping, pubmed-meshheading:20306460-Exons, pubmed-meshheading:20306460-Female, pubmed-meshheading:20306460-Humans, pubmed-meshheading:20306460-Male, pubmed-meshheading:20306460-Membrane Transport Proteins, pubmed-meshheading:20306460-Mutation, Missense, pubmed-meshheading:20306460-Pedigree, pubmed-meshheading:20306460-Pregnancy, pubmed-meshheading:20306460-Prenatal Diagnosis, pubmed-meshheading:20306460-Spastic Paraplegia, Hereditary
pubmed:year	2010
pubmed:articleTitle	Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't