Autori: Johnson Katherine
| Naslov | Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness (Article) |
| Autori | Johnson Katherine ... Rakocevic-Stojanovic Vidosava M Peric Stojan Z ... (broj koautora 17) |
| Info | ORPHANET JOURNAL OF RARE DISEASES, (2017), vol. 12 br. , str. - |
| Projekat | Sanofi Genzyme; Ultragenyx; Kurt + Peter Foundation; LGMD2I Research Fund; Samantha J Brazzo Foundation; LGMD2D Foundation; Muscular Dystrophy UK; Coalition to Cure Calpain 3; National Human Genome Research Institute; National Eye Institute; National Hear |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
