Associated Papers
Startle Disease: New Molecular Insights into an Old Neurological Disorder.
Schaefer N et al.
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry, 2023
The impact of human hyperekplexia mutations on glycine receptor structure and function.
Bode A et al.
Molecular Brain, 2014
GLRB is the third major gene of effect in hyperekplexia.
Chung SK et al.
Human Molecular Genetics, 2013
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