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

Author(s):
Quinn, P.M.; Mulder, A.A.; Alves, C.H.; Desrosiers, M.; Vries, S.I. de; Klooster, J.; Dalkara, D.; Koster, A.J. (0000-0003-1717-2549); Jost, C.R.; Wijnholds, J. (0000-0003-0099-460X)
Published
2019
Publication type
Article / Letter to editor
Date issued
2019-01-01
Language
English
Is part of
Human Molecular Genetics (2019), Vol. 28, no. 1, p. 105-123
hdl
1887/121059
doi
10.1093/hmg/ddy337