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Autor:
Zangrandi, Andreas Lieb, Germana Thaler, Barbara Fogli, Olga Trovato, Mitja Amon Posch, Teresa Kaserer, Luca
Publikováno v:
Biomedicines; Volume 9; Issue 12; Pages: 1882
Mutations in the prodynorphin gene (PDYN) are associated with the development of spinocerebellar ataxia type 23 (SCA23). Pathogenic missense mutations are localized predominantly in the PDYN region coding for the dynorphin A (DynA) neuropeptide and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::90fbb1b4f68f2c360cee772ba055331d
