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Paper Details

Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night Blindness.
Ophthalmic Res
1
2022
Arg292Ter, CSNB, Congenital stationary night blindness, Gln223Pro, Gly107Arg, Gly303ValfsTer45, NM_000541, NM_002905, NM_002905.4:c.668A, NYX, RDH5, SAG, c, c., c.319G>C, c.668A>C, c.874C>T, congenital stationary night blindness, electroretinogram (ERG, inherited retinal disorder, p.Gln223Pro, p.Gly107Arg
Author NameAffiliation
Mathieu QuinodozInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Mathieu QuinodozUniversity of Basel
Mathieu QuinodozUniversity of Leicester
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Basel
Carlo RivoltaUniversity of Leicester
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Basel
Carlo RivoltaUniversity of Leicester
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