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KITH_HHV23 Rabbit Polyclonal Antibody, 50ul PCR Series an autosomal dominant disorder characterized

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KITH_HHV23 Rabbit Polyclonal Antibody, 50ul PCR Series an autosomal dominant disorder characterized

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Description

an autosomal dominant disorder characterized by numerous small white flecks present in all layers of the corneal stroma

Was originally (PubMed:2480877) thought to be myoblast cell surface antigen 24

has been shown to play a central role in mediating the immune regulatory signal of this cytokine

Duplication of a regulatory region downstream of BMP2 causes a form of brachydactyly characterized by a malformed index finger and second toe in human patients

Involved in accumulation of zinc in synaptic vesicles

KITH_HHV23 Rabbit Polyclonal Antibody, 50ul PCR Series an autosomal dominant disorder characterized

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