神经科学论文(6).pdf
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European Journal of Neurology 2013, 20: 872 –878 doi:10.1111/ene.12104
REVIEW ARTICLE
PRRT2 mutations and paroxysmal disorders a,b,c a,c d,e a,b,c a,c,f
A. Meneret , C. Gaudebout , F. Riant , M. Vidailhet , C. Depienne and a,b,c
E. Roze
a INSERM, UMRS 975, et CNRS 7225 –CRICM, H o^pital Piti e-Salp e^tri e re, Paris; b Departement de Neurologie, AP-HP, Ho^ pital Piti e-
Salp ^etri ere, Paris; c Universit e Pierre et Marie Curie-Paris-6, Paris; d AP-HP, Groupe hospitalier Lariboisi ere-Fernand Widal, Laboratoire e f
de Genetique, Paris; INSERM UMR-S740; Universit e Paris 7 Denis Diderot, Paris; and Departement de Genetique et de Cytog enetique,
AP-HP, H o^ pital Piti e-Salp e^tri ere, Federation de Genetique, Paris, France
Keywords: In the past year, mutations in the PRRT2 gene have been id