C. Altuzarra
发表
L. Vercueil,
A. Afenjar,
S. Auvin,
2013,
Orphanet Journal of Rare Diseases.
O. Dulac,
C. Bulteau,
P. van Bogaert,
2009,
Epilepsia.
A. Munnich,
N. Boddaert,
A. Rötig,
2012,
American journal of human genetics.
A. Biraben,
L. Valton,
A. Vermersch,
2021,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
T. Dörk,
M. Stern,
P. Calvas,
2019,
Human mutation.
Ethan M. Goldberg,
Zara,
Silvana,
2021
.
A. Afenjar,
N. Philip,
D. Ville,
2015,
Epilepsia.
A. Verloes,
J. Vallat,
A. Echaniz-Laguna,
2021,
neurogenetics.
S. Julia,
A. Afenjar,
O. Dulac,
2019,
Epilepsia.
A. Afenjar,
I. Chantret,
S. Vuillaumier‐Barrot,
2011
.
C. Richelme,
P. Sabouraud,
S. Quijano-roy,
2020,
Orphanet Journal of Rare Diseases.
A. Munnich,
N. Boddaert,
T. Frebourg,
2011,
Human mutation.
A. Pagnamenta,
P. May,
W. van Paesschen,
2019,
Neurology.
P. May,
S. Knight,
D. Lowenstein,
2022
.
Wolfgang Müller-Felber,
Arnold Munnich,
Laurence Hubert,
2010,
Human mutation.
L. Gallagher,
E. Haffen,
C. Depienne,
2012,
Journal of Medical Genetics.
Ethan M. Goldberg,
S. Scherer,
J. Howe,
2021,
medRxiv.
F. Bartolomei,
P. Striano,
A. Coppola,
2021,
Brain : a journal of neurology.
G. Alcaraz,
A. Afenjar,
L. Aniksztejn,
2015,
Neurobiology of Disease.
A. Afenjar,
C. Barnérias,
P. de Lonlay,
2010,
Journal of Medical Genetics.
G. Alcaraz,
A. Afenjar,
L. Aniksztejn,
2015
.
A. Afenjar,
N. Philip,
D. Ville,
2015,
Epilepsia.
A. Pagnamenta,
P. May,
W. van Paesschen,
2019,
Neurology.