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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

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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)

Diseases associated with GP1BA include von willebrand disease

The ARPs are involved in diverse cellular processes

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

it probably only interacts with NFKBIB in vivo

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

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