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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype
RENAUD M; MOREIRA MC; BEN MONGA B; RODRIGUEZ D; DEBS R; CHARLES P; CHAOUCH M; FERRAT F; LAURENCIN C; VERCUEIL L; MALLARET M; M'ZAHEM A; PACHA LA; TAZIR M; TILIKETE C; OLLAGNON E; OCHSNER F; KUNTZER T; JUNG HH; BEIS JM; NETTER JC; DJAMSHIDIAN A; BOWER M; BOTTANI A; WALSH R; MURPHY S; REILEY T; BIETH E; ROELENS F; POLL-THE BT; LOURENCO CM; JARDIM LB; STRAUSSBERG R; LANDRIEU P; ROZE E; THOBOIS S; POUGET J; GUISSART C; GOIZET C; DURR A; TRANCHANT C; KOENIG M; ANHEIM M
JAMA NEUROL , 2018, vol. 75, n° 4, p. 495-502 Doc n°: 185442 D.O.I. : http://dx.doi.org/DOI:10.1001/jamaneurol.2017.4373 Descripteurs : AD62 - APRAXIE - DYSPRAXIE - ATAXIE Importance: Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal Langue : ANGLAIS |
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