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Detection and prenatal diagnosis for RS1 gene mutations in two Chinese families with X-linked juvenile retinoschisis / 中华医学遗传学杂志
Article in Zh | WPRIM | ID: wpr-237282
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To identify potential mutations of retinoschisis 1 (RS1) gene responsible for X-linked retinoschisis (XLRS) in two Chinese families.</p><p><b>METHODS</b>The 6 exons and flanking intronic regions were analyzed with PCR and direct sequencing.</p><p><b>RESULTS</b>Two RS1 mutations were identified in the two families, which included 1 frameshift mutation (c.573delG, p.Pro192fs) and 1 missense mutation (c.626G>A, p.Arg209His).</p><p><b>CONCLUSION</b>Two RS1 mutations have been identified, among which Pro192fs mutation is discovered for the first time in Chinese population. Above results may enrich our understanding of the clinical manifestations of XLRS and facilitated early diagnosis and genetic counseling for the disease.</p>
Subject(s)
Full text: 1 Index: WPRIM Main subject: Prenatal Diagnosis / Retinoschisis / Genetic Diseases, X-Linked / Diagnosis / Eye Proteins / Genetics / Mutation Type of study: Diagnostic_studies / Screening_studies Limits: Adolescent / Adult / Female / Humans / Male Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2013 Type: Article
Full text: 1 Index: WPRIM Main subject: Prenatal Diagnosis / Retinoschisis / Genetic Diseases, X-Linked / Diagnosis / Eye Proteins / Genetics / Mutation Type of study: Diagnostic_studies / Screening_studies Limits: Adolescent / Adult / Female / Humans / Male Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2013 Type: Article