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

Peter M Quinn, Aat A Mulder, C Henrique Alves, Mélissa Desrosiers, Sharon I de Vries, J. Klooster, Deniz Dalkara, Abraham J Koster, Carolina R Jost, J. Wijnholds

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Medicine & Life Sciences