Your browser doesn't support javascript.
loading
Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2 / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 325-328, 2004.
Article in Chinese | WPRIM | ID: wpr-328885
ABSTRACT
<p><b>OBJECTIVE</b>To use microsatellite DNA tightly linked to polycystic kidney disease gene 2 in the gene diagnosis of autosomal dominant polycystic kidney disease type 2.</p><p><b>METHODS</b>Microsatellite DNA of D4S1534, D4S1542, D4S1563,D4S2460 and D4S423 were amplified with PCR and the fragments of products were analyzed by capillary electrophoresis and Genescan and Genotyper software, and then gene diagnosis of the pedigrees was made by linkage analysis.</p><p><b>RESULTS</b>Three families were found to be linked to PKD2 in 20 families. Two carriers of PKD2 mutation were revealed by linkage analysis.</p><p><b>CONCLUSION</b>Gene diagnosis can be done for PKD2 mutation carriers prior to cytogenesis. Linkage analysis is a rapid, simple method for studying the heterogeneity of polycystic kidney disease and for diagnosing the disease at the molecular level.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Polycystic Kidney, Autosomal Dominant / Microsatellite Repeats / Diagnosis / TRPP Cation Channels / Genetics / Genetic Linkage / Mutation Type of study: Diagnostic study Limits: Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2004 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Polycystic Kidney, Autosomal Dominant / Microsatellite Repeats / Diagnosis / TRPP Cation Channels / Genetics / Genetic Linkage / Mutation Type of study: Diagnostic study Limits: Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2004 Type: Article