Respiratory decline is integral to disease progression in Huntington's disease

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Respiratory decline is integral to disease progression in Huntington's disease

Huntington’s disease is an autosomal inherited monogenetic condition in which the mutation is an expansion of the cytosine-adenine-guanine (CAG) repeat sequence at the N-terminal end of the huntingtin gene [1]. More than 40 repeats are associated with neuronal dysfunction and death, predominantly within the striatum resulting in a triad of movement, behaviour and cognitive impairment; other sym...

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ژورنال

عنوان ژورنال: European Respiratory Journal

سال: 2016

ISSN: 0903-1936,1399-3003

DOI: 10.1183/13993003.02215-2015