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Items: 2

1.

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

Quinn PM, Mulder AA, Henrique Alves C, Desrosiers M, de Vries SI, Klooster J, Dalkara D, Koster AJ, Jost CR, Wijnholds J.

Hum Mol Genet. 2019 Jan 1;28(1):105-123. doi: 10.1093/hmg/ddy337.

PMID:
30239717
2.

Crumbs 2 prevents cortical abnormalities in mouse dorsal telencephalon.

Dudok JJ, Murtaza M, Henrique Alves C, Rashbass P, Wijnholds J.

Neurosci Res. 2016 Jul;108:12-23. doi: 10.1016/j.neures.2016.01.001. Epub 2016 Jan 21.

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