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1 Ergebnisse
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ACTB gene mutation in combined Dystonia-Deafness syndrome w..:
Straccia, Giulia
;
Reale, Chiara
;
Castellani, Massimo
...
Parkinsonism & Related Disorders. 104 (2022) - p. 3-6 , 2022
Link:
https://doi.org/10.1016/j.parkreldis.2022.09.012
RT Journal T1
ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.parkreldis.2022.09.012&Exemplar=1&LAN=DE A1 Straccia, Giulia A1 Reale, Chiara A1 Castellani, Massimo A1 Colangelo, Isabel A1 Orunesu, Eva A1 Meoni, Sara A1 Moro, Elena A1 Krack, Paul A1 Prokisch, Holger A1 Zech, Michael A1 Romito, Luigi Michele A1 Garavaglia, Barbara PB Elsevier BV YR 2022 SN 1353-8020 JF Parkinsonism & Related Disorders VO 104 SP 3 OP 6 LK http://dx.doi.org/https://doi.org/10.1016/j.parkreldis.2022.09.012 DO https://doi.org/10.1016/j.parkreldis.2022.09.012 SF ELIB - SuUB Bremen
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