Huntington’s disease (HD) is a progressive, fatal, dominant inherited neurodegenerative disorder caused by an unstable expansion of CAG repeats within the coding region of the IT15 gene that encodes for a protein called huntingtin (htt). The clinical hallmark of HD is a severe motor impairment, but cognitive and psychiatric symptoms are early clinical features in HD that often appear before the onset of motor signs. This book discusses the prevalence, pathogenesis and treatment of HD.
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Formato PDF ● Páginas 200 ● ISBN 9781536108439 ● Editor Christina Hughes ● Editora Nova Science Publishers ● Publicado 2017 ● Carregável 3 vezes ● Moeda EUR ● ID 7216364 ● Proteção contra cópia Adobe DRM
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