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ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene are

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ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene areBelongs to the alkB family.

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Description

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex

Gene Ontology (GO) annotations related to this gene include peptide antigen binding and MHC class II receptor activity

Reduced activity of this enzyme may also play a role in ataxia-telangiectasia

ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene areBelongs to the alkB family.

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