Cognitive and Social Impairment in Mouse Models Mirrors Dravet Syndrome: Cognitive and Social Impairment in Dravet Mice
JA Kearney - Epilepsy Currents, 2013 - journals.sagepub.com
The models are an Scn1a+/-knockout mouse developed in the laboratory of Dr. William
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …
[HTML][HTML] Cognitive and Social Impairment in Mouse Models Mirrors Dravet Syndrome
JA Kearney - Epilepsy Currents, 2013 - ncbi.nlm.nih.gov
The models are an Scn1a+/-knockout mouse developed in the laboratory of Dr. William
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …
Cognitive and social impairment in mouse models mirrors dravet syndrome.
JA Kearney - Epilepsy Currents, 2013 - europepmc.org
Haploinsufficiency of the SCN1A gene encoding voltage-gated sodium channel NaV1. 1
causes Dravet syndrome, a childhood neuropsychiatric disorder that includes recurrent …
causes Dravet syndrome, a childhood neuropsychiatric disorder that includes recurrent …
[引用][C] Cognitive and social impairment in mouse models mirrors dravet syndrome
JA Kearney - Epilepsy currents, 2013 - pubmed.ncbi.nlm.nih.gov
[引用][C] Cognitive and social impairment in mouse models mirrors dravet syndrome
JA Kearney - Epilepsy Currents, 2013 - scholars.northwestern.edu
Cognitive and social impairment in mouse models mirrors dravet syndrome — Northwestern
Scholars Skip to main navigation Skip to search Skip to main content Northwestern Scholars …
Scholars Skip to main navigation Skip to search Skip to main content Northwestern Scholars …
Cognitive and social impairment in mouse models mirrors dravet syndrome.
JA Kearney - Epilepsy Currents, 2013 - europepmc.org
The models are an Scn1a+/-knockout mouse developed in the laboratory of Dr. William
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …
Catterall (4) and a mouse engineered with the Dravet syndrome mutation SCN1A-R1407X …