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Human Sterol regulatory element-binding protein 1C, SREBP-1C ELISA Kit, 96T ssDNA Synthesis Defects in this gene are

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Human Sterol regulatory element-binding protein 1C, SREBP-1C ELISA Kit, 96T ssDNA Synthesis Defects in this gene are

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Description

Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1)| also called X-linked congenital stationary night blindness (XLCSNB)

GO annotations related to this gene include nucleic acid binding and ubiquitin protein ligase binding

and hemostasis

May have a role in regulation of GABAergic transmission in the brain through the reuptake of GABA into presynaptic terminals

Human Sterol regulatory element-binding protein 1C, SREBP-1C ELISA Kit, 96T ssDNA Synthesis Defects in this gene are

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