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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

and in the formation of intramolecular interactions

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

CSA or DDB2

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

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

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