| pubmed-article:14592868 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14592868 | lifeskim:mentions | umls-concept:C0000768 | lld:lifeskim |
| pubmed-article:14592868 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:14592868 | lifeskim:mentions | umls-concept:C0751882 | lld:lifeskim |
| pubmed-article:14592868 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:14592868 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:14592868 | pubmed:dateCreated | 2003-10-31 | lld:pubmed |
| pubmed-article:14592868 | pubmed:abstractText | The objective was to define the molecular mechanisms underlying congenital myasthenic syndromes (CMS) by studying mutations within genes encoding the acetylcholine receptor (AChR) and related proteins at the neuromuscular junction. It was found that mutations within muscle AChRs are the most common cause of CMS. The majority are located within the epsilon-subunit gene and result in AChR deficiency. | lld:pubmed |
| pubmed-article:14592868 | pubmed:language | eng | lld:pubmed |
| pubmed-article:14592868 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14592868 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:14592868 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14592868 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14592868 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14592868 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:14592868 | pubmed:issn | 0077-8923 | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:BeesonDavidD | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:VincentAngela... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:Newsom-DavisJ... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:ColquhounDavi... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:CroxenRebecca... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:EalingJohnJ | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:WebsterRichar... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:BrownlowSharo... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:HattonChrisC | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:BrydsonMartin... | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:SlaterClarkeC | lld:pubmed |
| pubmed-article:14592868 | pubmed:author | pubmed-author:ShelleyChrisC | lld:pubmed |
| pubmed-article:14592868 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14592868 | pubmed:volume | 998 | lld:pubmed |
| pubmed-article:14592868 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14592868 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14592868 | pubmed:pagination | 114-24 | lld:pubmed |
| pubmed-article:14592868 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
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| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:meshHeading | pubmed-meshheading:14592868... | lld:pubmed |
| pubmed-article:14592868 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:14592868 | pubmed:articleTitle | Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes. | lld:pubmed |
| pubmed-article:14592868 | pubmed:affiliation | Neurosciences Group, Weatherall Institute of Molecular Medicine, The John Radcliffe, Headington, Oxford OX3 9DS, United Kingdom. dbeeson@hammer.imm.ox.ac.uk | lld:pubmed |
| pubmed-article:14592868 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:14592868 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:14592868 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1145 | entrezgene:pubmed | pubmed-article:14592868 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:14592868 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:14592868 | lld:pubmed |
