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CACNA1F inhibits ERG. 1 / 1
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"Mutations in CACNA1F, which encodes the Ca (v) 1.4 subunit of a voltage gated L-type calcium channel, cause X linked incomplete congenital stationary night blindness (CSNB2), a condition of defective retinal neurotransmission which results in night blindness, reduced visual acuity, and diminished ERG b-wave."