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Les mutations de novo dans PPP2R5D et NR4A2, deux nouvelles..:
Wirth, Thomas
;
Mariani, Louise-Laure
;
Hubsch, Cecile
...
Revue Neurologique. 177 (2021) - p. S49 , 2021
Link:
https://doi.org/10.1016/j.neurol.2021.02.188
RT Journal T1
Les mutations de novo dans PPP2R5D et NR4A2, deux nouvelles causes génétiques de syndrome parkinsonien précoce dopasensible
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.neurol.2021.02.188&Exemplar=1&LAN=DE A1 Wirth, Thomas A1 Mariani, Louise-Laure A1 Hubsch, Cecile A1 Tranchant, Christine A1 Chelly, Jamel A1 Roze, Emmanuel A1 Anheim, Mathieu PB Elsevier BV YR 2021 SN 0035-3787 JF Revue Neurologique VO 177 SP S49 LK http://dx.doi.org/https://doi.org/10.1016/j.neurol.2021.02.188 DO https://doi.org/10.1016/j.neurol.2021.02.188 SF ELIB - SuUB Bremen
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