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EBLN2 Rabbit Polyclonal Antibody, 50ul Enzymes Mutations in this gene are

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EBLN2 Rabbit Polyclonal Antibody, 50ul Enzymes Mutations in this gene are

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Description

Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens

Mutation in one of the family members (bestrophin 1) is associated with vitelliform macular dystrophy

The protein associates with several components of the extracellular signal-regulated kinase (ERK) pathway

The innate immune system recognizes microbial pathogens through Toll-like receptors (TLRs)

disease:Defects in CDKN2A are a cause of Li-Fraumeni syndrome (LFS)

EBLN2 Rabbit Polyclonal Antibody, 50ul Enzymes Mutations in this gene are

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