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MAFIP Rabbit Polyclonal Antibody, 100ul Filtration Defects in this gene are

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MAFIP Rabbit Polyclonal Antibody, 100ul Filtration Defects in this gene are

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Description

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

which participates in glycosylation and transport of proteins and lipids in the secretory pathway

Sialomucins are a heterogeneous group of secreted or membrane-associated mucins that appear to play 2 key but opposing roles in vivo: first as cytoprotective or antiadhesive agents

a peptide causing numerous physiological effects

and it plays a role in T-cell development and lymphocyte activation

MAFIP Rabbit Polyclonal Antibody, 100ul Filtration Defects in this gene are

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