Vincent, Ajoy <br/><br/>
Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.  [electronic resource] 

 -  American journal of human genetics  05 2016 
 - 1011-1019 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2016.03.021  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Animals<br/>Case-Control Studies<br/>Electroretinography<br/>Eye Diseases, Hereditary--etiology<br/>Female<br/>Genes, Recessive--genetics<br/>Genetic Diseases, X-Linked--etiology<br/>Genotype<br/>Heterotrimeric GTP-Binding Proteins--chemistry<br/>Homozygote<br/>Humans<br/>Male<br/>Mice<br/>Middle Aged<br/>Mutation--genetics<br/>Myopia--etiology<br/>Night Blindness--etiology<br/>Pedigree<br/>Phenotype<br/>Protein Conformation<br/>Sequence Homology, Amino Acid<br/>Visual Acuity--genetics