| pubmed-article:12324874 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12324874 | lifeskim:mentions | umls-concept:C2926606 | lld:lifeskim |
| pubmed-article:12324874 | lifeskim:mentions | umls-concept:C0917713 | lld:lifeskim |
| pubmed-article:12324874 | lifeskim:mentions | umls-concept:C2607943 | lld:lifeskim |
| pubmed-article:12324874 | lifeskim:mentions | umls-concept:C0017431 | lld:lifeskim |
| pubmed-article:12324874 | lifeskim:mentions | umls-concept:C1707520 | lld:lifeskim |
| pubmed-article:12324874 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:12324874 | pubmed:dateCreated | 2002-9-26 | lld:pubmed |
| pubmed-article:12324874 | pubmed:abstractText | To correlate the electroretinography (ERG) findings in patients with Duchenne/Becker muscular dystrophy (D/BMD) with the genotype and evaluate the ERG findings in DMD carriers. | lld:pubmed |
| pubmed-article:12324874 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12324874 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12324874 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12324874 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12324874 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12324874 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:12324874 | pubmed:issn | 1381-6810 | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:AfrashiFilizF | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:UlgenalpAyfer... | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:SöylevMeltem... | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:OnerF HakanFH | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:BoraElçinE | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:KöseSüheylaS | lld:pubmed |
| pubmed-article:12324874 | pubmed:author | pubmed-author:ErçalDeryaD | lld:pubmed |
| pubmed-article:12324874 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12324874 | pubmed:volume | 23 | lld:pubmed |
| pubmed-article:12324874 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12324874 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12324874 | pubmed:pagination | 157-65 | lld:pubmed |
| pubmed-article:12324874 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:meshHeading | pubmed-meshheading:12324874... | lld:pubmed |
| pubmed-article:12324874 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12324874 | pubmed:articleTitle | Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype. | lld:pubmed |
| pubmed-article:12324874 | pubmed:affiliation | Department of Pediatrics - Genetic Unit, Dokuz Eylül University, Izmir, Turkey. ayferulg@yahoo.com | lld:pubmed |
| pubmed-article:12324874 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12324874 | pubmed:publicationType | Comparative Study | lld:pubmed |
