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1 Ergebnisse
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De novo mutation screening in childhood-onset cerebellar at..:
Chemin, Jean
;
Siquier-Pernet, Karine
;
Nicouleau, Michaël
...
Brain. 141 (2018) 7 - p. 1998-2013 , 2018
Link:
https://doi.org/10.1093/brain/awy145
RT Journal T1
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_brain_awy145&Exemplar=1&LAN=DE A1 Chemin, Jean A1 Siquier-Pernet, Karine A1 Nicouleau, Michaël A1 Barcia, Giulia A1 Ahmad, Ali A1 Medina-Cano, Daniel A1 Hanein, Sylvain A1 Altin, Nami A1 Hubert, Laurence A1 Bole-Feysot, Christine A1 Fourage, Cécile A1 Nitschké, Patrick A1 Thevenon, Julien A1 Rio, Marlène A1 Blanc, Pierre A1 vidal, Céline A1 Bahi-Buisson, Nadia A1 Desguerre, Isabelle A1 Munnich, Arnold A1 Lyonnet, Stanislas A1 Boddaert, Nathalie A1 Fassi, Emily A1 Shinawi, Marwan A1 Zimmerman, Holly A1 Amiel, Jeanne A1 Faivre, Laurence A1 Colleaux, Laurence A1 Lory, Philippe A1 Cantagrel, Vincent PB Oxford University Press (OUP) YR 2018 SN 0006-8950 SN 1460-2156 JF Brain VO 141 IS 7 SP 1998 OP 2013 LK http://dx.doi.org/https://doi.org/10.1093/brain/awy145 DO https://doi.org/10.1093/brain/awy145 SF ELIB - SuUB Bremen
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