CABP4 Polyclonal Antibody, 100ul Microplate Mixer Defects in this gene may
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CABP4 Polyclonal Antibody, 100ul Microplate Mixer Defects in this gene mayThis gene encodes a member of the CABP family of calcium binding protein characterized by four EF hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene.
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