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De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia
| Naziv: | De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia | Autori  : | Van, de Vondel Liedewei; ...; Brankovic, Vesna; ...; (broj, koautora 38) | Godina: | 2022 | Publikacija: | MOVEMENT DISORDERS | ISSN: | 0885-3185 Movement Disorders Pretraži identifikator |
Tip rezultata: | Naučni članak | Kolacija: | vol. 37 br. 6 str. 1175-1186 | DOI: | 10.1002/mds.28959 | WoS-ID: | 000754310200001 | Scopus-ID: | 2-s2.0-85131821045 | URI: | https://enauka.gov.rs/handle/123456789/800815 | 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 |
Izvor metapodataka: | (Preuzeto iz Nasi u WoS) | M-kategorija: | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
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