Loss of CRB2 in Müller glial cells modifies a...

Human Molecular Genetics 2018 / 09

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

Quinn, Peter M, Mulder, Aat A, Henrique Alves, C, Desrosiers, Mélissa, Vries, Sharon I, Klooster, Jan, Dalkara, Deniz, Koster, Abraham J, Jost, Carolina R, Wijnholds, Jan
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Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddy337
Date:
September, 2018
File:
PDF, 2.06 MB
english, 2018
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