Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Stoker, Thomas B."'
Huntington’s disease (HD) is an autosomal dominant neurodegenerative condition caused by trinucleotide CAG repeat expansion in the huntingtin gene. CAG lengths of more than 35 repeats are associated with disease, whilst CAG lengths of less than 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e4c03639c9b0f25e9c2c6873bc04fc2
https://www.repository.cam.ac.uk/handle/1810/323650
https://www.repository.cam.ac.uk/handle/1810/323650
Autor:
Stoker, Thomas B, Barker, Roger A
Parkinson's disease is the second most common neurodegenerative disorder. It is characterised by a typical movement disorder that occurs in part because of the selective degeneration of the dopaminergic neurons of the substantia nigra pars compacta.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef1123c2fd0fb3b203fc8b7e1062262e
https://www.repository.cam.ac.uk/handle/1810/280538
https://www.repository.cam.ac.uk/handle/1810/280538