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The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italy
Autor:
Silvia Grimaldi, Livia Bernardi, Chiara Cupidi, Giuseppe Donato Mangano, Giuseppina Piccione, Raffaele Maletta, Salvatore Basiricò, Nicoletta Smirne, Enrico Grosso, Valentina Laganà, Amalia C. Bruni, Laura Orsi, Rosaria Nardello, Micaela Mitolo, Fabio Giacalone
BACKGROUND: Dentatorubral-pallidoluysian atrophy is a hereditary neurodegenerative disease prevalently reported in Japan but rare in Caucasians. The objective of this study was to reconstruct the pedigree of Italian dentatorubral-pallidoluysian atrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0088bc2f16058e219eecd9733cbf2019
http://hdl.handle.net/11585/876652
http://hdl.handle.net/11585/876652