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Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-287451

RESUMEN

<p><b>OBJECTIVE</b>To map the disease-causing gene in a Chinese family with autosomal dominant retinitis pigmentosa.</p><p><b>METHODS</b>Twenty-seven micro-satellite markers were randomly selected from the region around the known loci of causative genes, and haplotypes were determined by ABI3100 genetic analyzer. Two-point linkage analysis was performed using MLINK.</p><p><b>RESULTS</b>The Lod score of each marker vs adRP was below 1.</p><p><b>CONCLUSION</b>The phenotype of this family may not be caused by mutation of the known disease-causing genes.</p>


Asunto(s)
Femenino , Humanos , Masculino , Pueblo Asiatico , Genética , China , Genes Dominantes , Ligamiento Genético , Pruebas Genéticas , Repeticiones de Microsatélite , Genética , Mutación , Linaje , Fenotipo , Retinitis Pigmentosa , Diagnóstico , Genética , Patología
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