The Glycinergic System in Human Startle Disease: A Genetic Screening Approach

Human startle disease, also known as hyperekplexia (OMIM 149400), is a paroxysmal neurological disorder caused by defects in glycinergic neurotransmission. Hyperekplexia is characterised by an exaggerated startle reflex in response to tactile or acoustic stimuli which first presents as neonatal hype...

Descripción completa

Detalles Bibliográficos
Autores principales: Davies, Jeff S., Chung, Seo-Kyung, Thomas, Rhys H., Robinson, Angela, Hammond, Carrie L., Mullins, Jonathan G. L., Carta, Eloisa, Pearce, Brian R., Harvey, Kirsten, Harvey, Robert J., Rees, Mark I.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854534/
https://www.ncbi.nlm.nih.gov/pubmed/20407582
http://dx.doi.org/10.3389/fnmol.2010.00008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854534/
https://www.ncbi.nlm.nih.gov/pubmed/20407582
http://dx.doi.org/10.3389/fnmol.2010.00008

Ejemplares similares