about
A novel dominant hyperekplexia mutation Y705C alters trafficking and biochemical properties of the presynaptic glycine transporter GlyT2Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle diseaseDistinct phenotypes in zebrafish models of human startle disease.Molecular mechanisms of glycine transporter GlyT2 mutations in startle disease.
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Victoria M James
@ast
Victoria M James
@en
Victoria M James
@es
Victoria M James
@nl
type
label
Victoria M James
@ast
Victoria M James
@en
Victoria M James
@es
Victoria M James
@nl
prefLabel
Victoria M James
@ast
Victoria M James
@en
Victoria M James
@es
Victoria M James
@nl
P106
P21
P31
P496
0000-0002-9265-5914