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Study on mutation of presenilin-1 gene in familial Alzheimer's disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 455-458, 2004.
Artículo en Chino | WPRIM | ID: wpr-328851
ABSTRACT
<p><b>OBJECTIVE</b>To explore the role of the mutation of presenilin-1 exon 6 in pathogenesis of Alzheimer's disease(AD) patients.</p><p><b>METHODS</b>Exon 6 of presenilin-1 was analyzed by use of polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and DNA analyzer technique in 2 patients with familial AD, 53 patients with sporadic DA, 60 patients with vascular dementia(VD) and 90 normal controls.</p><p><b>RESULTS</b>Mobility shift of SSCP in exon 6 of presenilin-1 was detected in 2 cases with FAD, 4 cases with SDA and 1 case with VD. Two missense mutations were found in the patients by DNA sequence analysis, one mutation was 1123 nt C-->G(Cys 23 Trp) and the other was 1300 nt A-->C(Asp 200 Ala).</p><p><b>CONCLUSION</b>Mutations in exon 6 of presenilin-1 existed in the patients with FAD and SDA, and the two missense mutations were probably pathological by nature.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Reacción en Cadena de la Polimerasa / Exones / Análisis de Secuencia de ADN / Polimorfismo Conformacional Retorcido-Simple / Mutación Missense / Presenilina-1 / Enfermedad de Alzheimer / Genética / Mutación Límite: Anciano / Aged80 / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Reacción en Cadena de la Polimerasa / Exones / Análisis de Secuencia de ADN / Polimorfismo Conformacional Retorcido-Simple / Mutación Missense / Presenilina-1 / Enfermedad de Alzheimer / Genética / Mutación Límite: Anciano / Aged80 / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo