PMC:3654953 / 28806-29129 JSONTXT

{"project":"AxD_symptoms","denotations":[{"id":"T70","span":{"begin":144,"end":162},"obj":"Phenotype"},{"id":"T71","span":{"begin":167,"end":193},"obj":"Phenotype"}],"attributes":[{"id":"A70","pred":"hp_id","subj":"T70","obj":"http://purl.obolibrary.org/obo/HP_0100022"},{"id":"A71","pred":"hp_id","subj":"T71","obj":"http://purl.obolibrary.org/obo/HP_0002180"}],"text":"This work was supported by Fondazione Telethon grants GGP11011 and GPP10005; CARIPLO grant 2011/0526. The Cell lines and DNA bank of Paediatric Movement Disorders and Neurodegenerative Diseases, member of the Telethon Network of Genetic Biobanks (project no. GTB12001), funded by Telethon Italy, provided us with specimens."}