Zobrazeno 1 - 2
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pro vyhledávání: '"Gabe Kringlen"'
Publikováno v:
Journal of Huntington's disease. 6(4)
Background Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. In most cases the disease is inherited from a parent, although a considerable number of affected persons have no reported family history of the disease. While C
Autor:
Kringlen, Gabe1,2 kringleng@gmail.com, Kinsley, Lisa1,3, Aufox, Sharon1,4, Rouleau, Gerald5, Bega, Danny3
Publikováno v:
Journal of Huntington's Disease. 2017, Vol. 6 Issue 4, p327-335. 9p.