Autori: Van de Vondel Liedewei
| Naslov | De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia (Article) |
| Autori | Van de Vondel Liedewei ... Brankovic Vesna ... (broj koautora 38) |
| Info | MOVEMENT DISORDERS, (2022), vol. 37 br. 6, str. 1175-1186 |
| Projekat | European Reference Network for Rare Neuromuscular Diseases (ERN EURO-NMD) [870177]; EJPRD PREPARE Consortium; EJPRD PROSPAX consortium (EJP RD COFUND-EJP) [825575]; SPATAX network; TreatHSP network; European Reference Network for Rare Neurological Disease |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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