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Linkage analysis of one family with autosomal dominant high myopia / 中华医学遗传学杂志
Article de Zh | WPRIM | ID: wpr-308048
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To map the high myopia gene in a Chinese family with autosomal dominant high myopia.</p><p><b>METHODS</b>A family with autosomal dominant high myopia in three generations was collected. Eighteen short-tandem-repeat markers on previously reported loci linked to high myopia were chosen for genotyping and two-point linkage analysis was carried out.</p><p><b>RESULTS</b>The spherical equivalent of affected individuals ranges from -6.00D to -20.00D and the genetic pattern is autosomal dominant. The LOD score was less than -1 in all 18 microsatellite markers, indicating that there was no linkage between these markers and the high myopia related genes in this family.</p><p><b>CONCLUSION</b>A novel myopia locus for high-grade myopia may exist in the kindred. Genome-wide scan will be needed to determine this novel locus.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pedigree / Physiologie / Réfraction oculaire / Répétitions microsatellites / Polymorphisme de nucléotide simple / Génétique / Liaison génétique / Lod score / Myopie Limites du sujet: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male langue: Zh Texte intégral: Chinese Journal of Medical Genetics Année: 2008 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pedigree / Physiologie / Réfraction oculaire / Répétitions microsatellites / Polymorphisme de nucléotide simple / Génétique / Liaison génétique / Lod score / Myopie Limites du sujet: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male langue: Zh Texte intégral: Chinese Journal of Medical Genetics Année: 2008 Type: Article