Persistent URL of this record https://hdl.handle.net/1887/121059
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Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
- All authors
- Quinn, P.M.; Mulder, A.A.; Alves, C.H.; Desrosiers, M.; Vries, S.I. de; Klooster, J.; Dalkara, D.; Koster, A.J.; Jost, C.R.; Wijnholds, J.
- Date
- 2019-01-01
- Journal
- Human Molecular Genetics
- Volume
- 28
- Issue
- 1
- Pages
- 105 - 123