| pubmed-article:17880784 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17880784 | lifeskim:mentions | umls-concept:C0079259 | lld:lifeskim |
| pubmed-article:17880784 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:17880784 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:17880784 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:17880784 | lifeskim:mentions | umls-concept:C0008565 | lld:lifeskim |
| pubmed-article:17880784 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:17880784 | pubmed:dateCreated | 2007-9-20 | lld:pubmed |
| pubmed-article:17880784 | pubmed:abstractText | Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused by dystrophin gene mutations; 55%-65% of these pathogenic mutations are large deletion and duplication mutations that can be detected by multiplexed polymerase chain reaction. However, finding the remaining micro-mutations (substitutions, deletions or insertions of one or several nucleotides) cannot be achieved in this way. The aim of the present study was to detect mutations of the dystrophin gene in individuals with Duchenne muscular dystrophy (DMD) by denaturing high-performance liquid chromatography (DHPLC) and to establish a rapid and sensitive screening platform for micro-mutations leading to DMD. | lld:pubmed |
| pubmed-article:17880784 | pubmed:language | chi | lld:pubmed |
| pubmed-article:17880784 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880784 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17880784 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880784 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17880784 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:17880784 | pubmed:issn | 0578-1310 | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:KlosIu SIuS | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:VoelGG | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:LiNingN | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:ZhouXinX | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:ZhangXueX | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:JinChun-lianC... | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:LinChang-kunC... | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:ChenYa-nanYN | lld:pubmed |
| pubmed-article:17880784 | pubmed:author | pubmed-author:CaoLi-huaLH | lld:pubmed |
| pubmed-article:17880784 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17880784 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:17880784 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17880784 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17880784 | pubmed:pagination | 413-6 | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:meshHeading | pubmed-meshheading:17880784... | lld:pubmed |
| pubmed-article:17880784 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17880784 | pubmed:articleTitle | [Detection of new mutations in the dystrophin gene by denaturing high-performance liquid chromatography]. | lld:pubmed |
| pubmed-article:17880784 | pubmed:affiliation | The Research Center for Human Genomics and MOH Key Laboratory of Cell Biology, China Medical University, Shenyang 110001, China. | lld:pubmed |
| pubmed-article:17880784 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17880784 | pubmed:publicationType | English Abstract | lld:pubmed |
