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The Last Destiny. Assessment of Mutation Genetics in HTT (High Repetition-CAG), Gene for induced Huntington's disease
В наличии
Местонахождение: Алматы | Состояние экземпляра: новый |
Бумажная
версия
версия
Автор: Shahin Asadi
ISBN: 9783330004627
Год издания: 2016
Формат книги: 60×90/16 (145×215 мм)
Количество страниц: 228
Издательство: LAP LAMBERT Academic Publishing
Цена: 43696 тг
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Аннотация: 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.
Ключевые слова: genetic study, Huntington's disease (HD), Mutation The gene HTT