Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
isPeerReviewed
abstract
<p>Variations in the human Cru ...... rds an LCA-like phenotype.</p>
@en
authorList
type
label
Loss of CRB2 in Müller glial c ...... congenital amaurosis phenotype
category
electronicVersions
journalAssociation
keywordGroups
language
managingOrganisationalUnit
openAccessPermission
organisationalUnits
publicationStatuses
totalScopusCitations
visibility
Publiek - Geen beperking
@nl
workflow
Validated
@en