about
Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndromeManipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disordersTreatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jose A Herrera
@ast
Jose A Herrera
@en
Jose A Herrera
@es
Jose A Herrera
@nl
type
label
Jose A Herrera
@ast
Jose A Herrera
@en
Jose A Herrera
@es
Jose A Herrera
@nl
prefLabel
Jose A Herrera
@ast
Jose A Herrera
@en
Jose A Herrera
@es
Jose A Herrera
@nl
P106
P1153
56589494500
P21
P31
P496
0000-0003-3808-1769