Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Ozge Begli"'
Autor:
Anooshay Khan, Esra Yuca, Cemile Elif Özçelik, Ozge Begli, Oguzhan Oguz, Serkan Kasırga, Urartu Ozgur Safak Seker
Huntington’s disease (HD) is a progressive, autosomal dominant neurodegenerative disorder resulting from a significant amplification of CAG repeats in exon 1 of the Huntingtin (Htt) gene. More than 36 CAG repeats result in the formation of mutant H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76b9b89b10b5181fbc5f60af4125272f
https://doi.org/10.1101/2023.04.27.538016
https://doi.org/10.1101/2023.04.27.538016
