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Summary Literature (0)
MIM:616389 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G

Xenbase Genes: gnat1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014614 - cervical spinal cord white matter
MONDO:0016293 - congenital stationary night blindness