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Whole Genome Sequencing Identifies Missense Mutation in GRM6 as the Likely Cause of Congenital Stationary Night Blindness in a Tennessee Walking Horse
BioProject SRA
Blood - Congenital stationary night blindness, CSNB - Patient 2
Blood - Congenital stationary night blindness, CSNB - Patient 1
Genomic DNA extracted from peripheral blood of a CSNB patient
BioProject
OMIA001486-9615 - Night blindness, congenital stationary, LRIT3-related in Canis lupus familiaris (dog) [9615]
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