about
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problemsNeuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy.Deletion of murine Arv1 results in a lean phenotype with increased energy expenditure.CRISPR/Cas9: at the cutting edge of hepatology.Somatic genome editing with CRISPR/Cas9 generates and corrects a metabolic disease.Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral ProblemsIn Vivo Ryr2 Editing Corrects Catecholaminergic Polymorphic Ventricular TachycardiaSomatic Editing of Ldlr With Adeno-Associated Viral-CRISPR Is an Efficient Tool for Atherosclerosis Research
P50
Q24294551-CC0D9024-E6EB-4FE6-B0D8-5E46490A4D87Q36043147-621C48EE-68E8-4057-BA19-D41D24E29DE2Q36245523-7E534F26-FA0D-4B82-92A7-7C9142AFC0CBQ39294371-6A777B72-F5D0-4746-998E-9FA35A788F78Q41964540-BA94B54B-D144-4D58-AED7-BB3A8145487CQ57079523-886820D2-BCFE-4835-AE8E-FC7E43A3216CQ57820983-19BF721E-BD67-42EE-956B-362683DF085BQ90349121-C4BFB9DE-B38D-497A-A0E0-8B6B2AF91BCE
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-5358-8280
@en
name
Kelsey Jarrett
@ast
Kelsey Jarrett
@en
Kelsey Jarrett
@es
Kelsey Jarrett
@nl
type
label
Kelsey Jarrett
@ast
Kelsey Jarrett
@en
Kelsey Jarrett
@es
Kelsey Jarrett
@nl
prefLabel
Kelsey Jarrett
@ast
Kelsey Jarrett
@en
Kelsey Jarrett
@es
Kelsey Jarrett
@nl
P106
P1153
57191375339
P31
P496
0000-0001-5358-8280