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ZN776 Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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ZN776 Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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Description

Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10)

HLX is a Protein Coding gene

Members of this family are cell surface glycoproteins with a single IgV-like extracellular domain

Diseases associated with SERINC3 include hiv-1 and carbuncle

Three isoforms of cortactin exist due to the alternative splicing

ZN776 Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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