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DNA mismatch repair enzyme hMSH2 genetic polymorphism in southern Chinese Han population / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 256-258, 2003.
Artículo en Chino | WPRIM | ID: wpr-248444
ABSTRACT
<p><b>OBJECTIVE</b>To study hMSH2 genetic polymorphism in southern Chinese Han population.</p><p><b>METHODS</b>The basic materials and blood samples from 163 southern Chinese were collected. The mutations of exon 6 and exon 7 of hMSH2 gene were investigated by PCR-SSCP, followed by DNA sequencing.</p><p><b>RESULTS</b>Fragments of 250 bp including exon 6 and fragments of 323 bp including exon 7 of hMSH2 gene were amplified by multiple PCR. The allele frequencies of C18, A82 and B39 type mutations were 0.0184, 0.0031, 0.0031, respectively. The gene frequencies and gene type frequencies of three polymorphism sites in normal population accorded with Hardy-Weinberg equilibrium (P>0.05). The heterozygosity of C18 type mutation (0.0361) was the highest.</p><p><b>CONCLUSION</b>There were three polymorphism sites in exon 7 of hMSH2 gene in southern Chinese Han population, among which the genotype frequency of C18 type was the highest, suggesting that C18 type mutation be a useful genetic mark.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fisiología / ADN Ligasas / Polimorfismo Genético / Exones / Repeticiones de Microsatélite / Disparidad de Par Base / Enzimas Reparadoras del ADN / Pueblo Asiatico / Reparación de la Incompatibilidad de ADN / ADN Ligasa (ATP) Límite: Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2003 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fisiología / ADN Ligasas / Polimorfismo Genético / Exones / Repeticiones de Microsatélite / Disparidad de Par Base / Enzimas Reparadoras del ADN / Pueblo Asiatico / Reparación de la Incompatibilidad de ADN / ADN Ligasa (ATP) Límite: Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2003 Tipo del documento: Artículo