Zobrazeno 1 - 1
of 1
pro vyhledávání: '"I U, Larsen"'
Autor:
T, Vinther-Jensen, T T, Nielsen, E, Budtz-Jørgensen, I U, Larsen, M M, Hansen, L, Hasholt, L E, Hjermind, J E, Nielsen, A, Nørremølle
Publikováno v:
Clinical genetics. 89(3)
Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder characterized by motor, psychiatric, and cognitive manifestations. HD is caused by a CAG repeat expansion in the Huntingtin (HTT) gene but the exact pathogenesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f36822f44e3bec6fd7ba58ff48084f0
https://pubmed.ncbi.nlm.nih.gov/26081309
https://pubmed.ncbi.nlm.nih.gov/26081309
