Fr. 89.00

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

English, German · Paperback / Softback

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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.

About the author










Prof. Shahin Asadi (doctorat en génétique médicale et postdoctorat en neurogénétique - optogénétique). Je travaille dans le domaine de la génétique médicale du système nerveux humain et de la mémoire génétique humaine. Jusqu'à aujourd'hui, j'ai écrit et publié de nombreux livres et articles dans le domaine de la génétique du système nerveux humain et de la mémoire génétique humaine.

Product details

Authors Shahin Asadi
Publisher LAP Lambert Academic Publishing
 
Languages English, German
Product format Paperback / Softback
Released 02.12.2016
 
EAN 9783330004627
ISBN 978-3-33-000462-7
No. of pages 228
Subject Natural sciences, medicine, IT, technology > Biology > Genetics, genetic engineering

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