Autori: Tedesco Barbara
| Naslov | Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models (Article; Early Access) |
| Autori | Tedesco Barbara Peric Stojan Z ... Rakocevic-Stojanovic Vidosava M Milenkovic Sanja M ... Ivanovic Vukan ... (broj koautora 23) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. br. , str. - |
| Projekat | Sanofi Genzyme; Ultragenyx; LGMD2I Research Fund; Samantha J Brazzo Foundation; LGMD2D Foundation; Kurt+Peter Foundation; Muscular Dystrophy UK; Coalition to Cure Calpain 3; National Human Genome Research Institute [R01 HG009141]; National Eye Institute; National Heart, Lung and Blood Institute [UM1 HG008900]; Ministry of Science of the Republic of Serbia [175083]; Fondazione Telethon, Italy [GGP19128]; Fondazione Italiana per la ricercasulla Sclerosi Laterale Amiotrofica (AriSLA), Italy; Association Francaise contre les Myopathies (AFM Telethon), France [23236]; Italian Ministry of University and Research (MIUR) [2017F2A2C5, 2022EFLFL8]; European Union-Next Generation EU [CN00000041, CUPB93D21010860004]; Progetto Dipartimenti di Eccellenza; Universita degli Studi di Milano; Agenzia Italiana del Farmaco (AIFA); National Institute Of Arthritis And Musculoskeletal And Skin Diseases of the National Institutes of Health [R21AR080407]; UCL/UCLH Biomedicine NIHR, UK; University of Antwerp (TOP-BOF) [38694, 41667]; Flanders Fund for Scientific Research (FWO-Flanders) [G040821N]; Solve-RD [779257] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
