Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

PM Quinn, AA Mulder, C Henrique Alves… - Human Molecular …, 2019 - academic.oup.com
Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early onset of retinitis pigmentosa (RP) and Leber congenital …
被引用次数：47 相关文章

[引用][C] Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

PM Quinn, AA Mulder, CH Alves… - Human …, 2019 - scholarlypublications …
Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype
into a Leber congenital amaurosis phenotype | Scholarly Publications Skip to main content …

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.

PM Quinn, AA Mulder, CH Alves… - Human Molecular …, 2019 - search.ebscohost.com
Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early onset of retinitis pigmentosa (RP) and Leber congenital …

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

PM Quinn, AA Mulder, CH Alves… - Human Molecular …, 2019 - pure.knaw.nl
Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early-onset of retinitis pigmentosa (RP) and Leber congenital …

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

PM Quinn, AA Mulder, CH Alves… - Human molecular …, 2019 - pubmed.ncbi.nlm.nih.gov
Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early onset of retinitis pigmentosa (RP) and Leber congenital …

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.

PM Quinn, AA Mulder, H Alves… - Human Molecular …, 2019 - europepmc.org
Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early onset of retinitis pigmentosa (RP) and Leber congenital …

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

PM Quinn, AA Mulder, CH Alves, M Desrosiers… - Human Molecular …, 2018 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Variations in the human Crumbs homolog-1
(CRB1) gene lead to an array of retinal dystrophies including early onset of retinitis …