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f9715f56-22e7-44cb-9cbd-53d1d4cbac5d
f9715f56-22e7-44cb-9cbd-53d1d4cbac5d
http://hdl.handle.net/f9715f56-22e7-44cb-9cbd-53d1d4cbac5d
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
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f9715f56-22e7-44cb-9cbd-53d1d4cbac5d
http://hdl.handle.net/f9715f56-22e7-44cb-9cbd-53d1d4cbac5d