izvor podataka: crosbi
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Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism (CROSBI ID 313362)
Prilog u časopisu | Pismo uredniku | međunarodna recenzija
Perković, Romana ; Jerčić, Kristina Gotovac ; Frančić, Manuela ; Ozretić, David ; Borovečki, Fran
Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism // Acta neurologica Belgica, Online first (2022), 35980504, 5. doi: 10.1007/s13760-022-02064-2
Podaci o odgovornosti
Perković, Romana ; Jerčić, Kristina Gotovac ; Frančić, Manuela ; Ozretić, David ; Borovečki, Fran
engleski
Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism
Abstract
Frontotemporal dementia ; GRN mutation ; Parkinsonism ; Progranulin
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o izdanju
Online first
2022.
35980504
5
objavljeno
0300-9009
2240-2993
10.1007/s13760-022-02064-2
