The Last Destiny

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Assessment of Mutation Genetics in HTT (High Repetition-CAG), Gene for induced Huntington’s disease

ISBN: 3330004622
ISBN 13: 9783330004627
Autor: Asadi, Shahin
Verlag: LAP LAMBERT Academic Publishing
Umfang: 228 S.
Erscheinungsdatum: 02.12.2016
Auflage: 1/2016
Format: 1.5 x 22 x 15
Gewicht: 358 g
Produktform: Kartoniert
Einband: Kartoniert
Artikelnummer: 715658 Kategorie:

Beschreibung

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.

Autorenporträt

Shahin Asadi, Mina Niknia, students of Molecular Genetics, studied Molecular Biology at Tabriz Islamic Azad University Sciences. Bachelor Molecular and Cellular Biology-Genetics,Midwifery (Tocology) Master of Molecular Biology and Genetics Director of research, Nuclear Researcher of the National Center for Genetic Engineering and Biotechnology in Iran.

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