The Last Destiny : Assessment of Mutation Genetics in HTT (High Repetition-CAG), Gene for induced Huntington's disease

ISBN-13: 9783330004627 / Angielski / Miękka / 2016 / 228 str.

Shahin Asadi

Opis

Today, neurological disorders, neuromuscular disorders are very important in creating. Including neurological disorders,including Huntington's disease (HD). Huntington's disease (HD) are a neuromuscular disorder that commonly causes a progressive neurodegenerative disease with autosomal dominant inheritance, with the incidence in adulthood, the disease has three abnormal movements, cognitive disorders, psychological disorders known. Huntington's disease (HD) is caused by genetic mutations, but also epigenetic factors are critical in inducing the disease. In this study we have analyzed 120 people. 59 Huntington's disease (HD) and 61 control group. The gene HTT analyzed in terms of genetic mutation made. In this study,people who have genetic mutation were targeted, with nervous disorders, Huntington's disease (HD). In fact, of all people with Huntington's disease (HD), 59 Huntington's disease (HD) had a genetic mutation in the gene HTT Huntington's disease (HD). Any genetic mutations in the target genes control group, did not show. This is Last Destiny.

O autorze

Shahin Asadi,student of Molecular Genetics, studied Molecular Biology at Tabriz Islamic Azad University Sciences. Bachelor Molecular and Cellular Biology-Genetics,Master of Molecular Biology and Genetics Director of Research, Nuclear Molecular Cell Biology-Genetics Researcher of the National Center for Genetic Engineering and Biotechnology in Iran.