| pubmed-article:21613359 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C0000726 | lld:lifeskim |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C1333944 | lld:lifeskim |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C0205145 | lld:lifeskim |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C0206530 | lld:lifeskim |
| pubmed-article:21613359 | lifeskim:mentions | umls-concept:C1823386 | lld:lifeskim |
| pubmed-article:21613359 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:21613359 | pubmed:dateCreated | 2011-8-5 | lld:pubmed |
| pubmed-article:21613359 | pubmed:abstractText | Hereditary pheochromocytoma is associated with germline mutations of a set of susceptibility genes to which the TMEM127 gene has recently been added. Patients with TMEM127 mutations have been thus far exclusively identified with adrenal tumors. | lld:pubmed |
| pubmed-article:21613359 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21613359 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21613359 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:21613359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21613359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21613359 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21613359 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:21613359 | pubmed:issn | 1945-7197 | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:NeumannHartmu... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:EngCharisC | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:SchmidKurt... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:WalzMartin... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:HoffmannMicha... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:BertzHartmutH | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:MoellerLars... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:BoedekerCarst... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:SullivanMaren... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:WinterAurelia... | lld:pubmed |
| pubmed-article:21613359 | pubmed:author | pubmed-author:MalinocAngeli... | lld:pubmed |
| pubmed-article:21613359 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21613359 | pubmed:volume | 96 | lld:pubmed |
| pubmed-article:21613359 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21613359 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21613359 | pubmed:pagination | E1279-82 | lld:pubmed |
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| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:meshHeading | pubmed-meshheading:21613359... | lld:pubmed |
| pubmed-article:21613359 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21613359 | pubmed:articleTitle | Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites. | lld:pubmed |
| pubmed-article:21613359 | pubmed:affiliation | Department of Nephrology and General Medicine, University Medical Center, Albert-Ludwigs-University, Freiburg, Germany. hartmut.neumann@uniklinik-freiburg.de | lld:pubmed |
| pubmed-article:21613359 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21613359 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:55654 | entrezgene:pubmed | pubmed-article:21613359 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21613359 | lld:entrezgene |
