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Mody genes; linkage analysis and subgroup discovery from text documents
Professional Medical Journal-Quarterly [The]. 2013; 20 (4): 623-633
em Inglês | IMEMR | ID: emr-138461
ABSTRACT
Genetic screening of Maturity Onset Diabetes of the Young [MODY] genes has not been performed in Pakistan so far; albeit MODY genes have been noticed in local population. A relevant research will help to establish a scheme for identification and treatment of MODY. The data source for the subgroup discovery was retrieved from PubMed. Family affected by MODY were contacted personaly for descriptive study. The family history was obtained from the representative members of the family and pedigree was drawn. The extensive clinical examination of both patients and their unaffected normal relatives was carried out by expert clinician. Specific primers for region of interest in genomic DNA were designed at the IBGE Islamabad using Primer 3 during last quarter of 2011. Mutation detection was performed followed by pattern discovery using subgroup discovery technique. Unidentified MODY genes facilitating the cause of a specific diabetes in European population may play a central role for diabetes characterized by autosomal dominant transmission in Pakistani population. Exclusion study indicates that there is no linkage to the known loci of MODY. Similarly genetic screening results suggest that no mutation is indicated in this examined family in MODY genes. There may be some environmental factors involved in causing this disease in this family; otherwise this disease is due to mutation in other reported MODY genes which are not screened in this study. Subgroup discovery results point out that all the reported MODY genes have association among themselves revealing 580 patterns
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Polimorfismo Genético / Testes Genéticos / Programas de Rastreamento / Reação em Cadeia da Polimerase / Coleta de Dados / Predisposição Genética para Doença / Ligação Genética / Mutação Tipo de estudo: Estudo de rastreamento Limite: Humanos Idioma: Inglês Revista: Professional Med. J.-Q Ano de publicação: 2013

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Polimorfismo Genético / Testes Genéticos / Programas de Rastreamento / Reação em Cadeia da Polimerase / Coleta de Dados / Predisposição Genética para Doença / Ligação Genética / Mutação Tipo de estudo: Estudo de rastreamento Limite: Humanos Idioma: Inglês Revista: Professional Med. J.-Q Ano de publicação: 2013