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Five coding region polymorphism of mitochondrial DNA in Chinese Han population of Yanbian area / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 696-700, 2009.
Artículo en Chino | WPRIM | ID: wpr-349077
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the mitochondrial DNA (mtDNA) five coding region sequence polymorphisms encompassing positions nt3954-4506, nt5218-5974, nt7942-8711, nt10296-10653, and nt14496-14867 in Chinese Han population of Yanbian area, Jilin province.</p><p><b>METHODS</b>Polymerase chain reaction (PCR) and direct sequencing method were used to detect the haplotype distribution of mtDNA coding region in 200 unrelated Chinese Han individuals.</p><p><b>RESULTS</b>One hundred and ten haplotypes were observed in the 200 individuals. The gene diversity was 0.9879 and the random match probability was 0.0171. Compared with the Anderson's sequence,81 nucleotide variants were obtained,of which 66 were previously registered in MITOMAP,and 15 were novel.</p><p><b>CONCLUSION</b>The obtained data suggest that these sequence polymorphisms are valuable genetic markers for personal identification when added to mtDAN control region investigation, and thus could be used as basic data for the forensic application in Chinese Han population.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / ADN Mitocondrial / Datos de Secuencia Molecular / Secuencia de Bases / China / Sistemas de Lectura Abierta / Análisis de Secuencia de ADN / Pueblo Asiatico / Etnología / Genética Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2009 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / ADN Mitocondrial / Datos de Secuencia Molecular / Secuencia de Bases / China / Sistemas de Lectura Abierta / Análisis de Secuencia de ADN / Pueblo Asiatico / Etnología / Genética Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2009 Tipo del documento: Artículo