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GC224 Rabbit Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in CDKN1B are associated

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GC224 Rabbit Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in CDKN1B are associated

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Description

Mutations in CDKN1B are associated with multiple endocrine neoplasia type IV (MEN4)

It may have a role in the development of fragile X mental retardation syndrome

which suggests an essential role of this gene in the immune response to antigenic stimuli

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The encoded preproprotein is proteolytically processed to generate a subunit of the dimeric activin and inhibin protein complexes

GC224 Rabbit Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in CDKN1B are associated

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