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Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are
Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are
Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are
Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are

Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are

SKU: 82593467900

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Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges 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)

Pseudogenes have been identified on chromosomes 3 and 20

This receptor subunit forms an active heterodimeric complex with GABA-B receptor subunit 1

and plays a key role in the function of the PDH complex

Smad2/3 (Acetyl Lys420/378) Rabbit Polyclonal Antibody, 50ul Centrifuges Defects in this gene are

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