A Novel Heterozygous Missense Mutation in<i> GNAT1</i> Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

<div>Localization of wild-type GNAT1 and mutated variants overexpressed in COS-1 cells. The wild-type and mutant GNAT1 protein was detected by a mouse GNAT1 antibody (red). The nuclei were stained with DAPI (blue).</div>

BioMed Research International

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Figure 3

Figure 3: A Novel Heterozygous Missense Mutation in<i> GNAT1</i> Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness 

BioMed Research International

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

Figure 3