| pubmed-article:21835055 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C0021289 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C0020550 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C0034844 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C0206530 | lld:lifeskim |
| pubmed-article:21835055 | lifeskim:mentions | umls-concept:C0678257 | lld:lifeskim |
| pubmed-article:21835055 | pubmed:dateCreated | 2011-8-12 | lld:pubmed |
| pubmed-article:21835055 | pubmed:abstractText | Constitutively activating germline mutations in the thyrotropin receptor (TSHR) gene result in non-autoimmune hyperthyroidism and can be transmitted as a dominant trait or occur sporadically. These mutations are mostly located in the serpentine part of this G-protein coupled receptor. | lld:pubmed |
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| pubmed-article:21835055 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21835055 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21835055 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:21835055 | pubmed:issn | 1756-6614 | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:KrudeHeikoH | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:BiebermannHei... | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:GrütersAnnett... | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:KleinauGunnar... | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:WinklerFranzi... | lld:pubmed |
| pubmed-article:21835055 | pubmed:author | pubmed-author:HandkeDaniela... | lld:pubmed |
| pubmed-article:21835055 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21835055 | pubmed:volume | 4 Suppl 1 | lld:pubmed |
| pubmed-article:21835055 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21835055 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21835055 | pubmed:pagination | S8 | lld:pubmed |
| pubmed-article:21835055 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21835055 | pubmed:articleTitle | Molecular description of non-autoimmune hyperthyroidism at a neonate caused by a new thyrotropin receptor germline mutation. | lld:pubmed |
| pubmed-article:21835055 | pubmed:affiliation | Institute of Experimental Paediatric Endocrinology, Charité Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. heike.biebermann@charite.de. | lld:pubmed |
| pubmed-article:21835055 | pubmed:publicationType | Journal Article | lld:pubmed |
