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DFNA5 Polyclonal Antibody, 50ul Variant Libraries The homeobox A1 may be

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DFNA5 Polyclonal Antibody, 50ul Variant Libraries The homeobox A1 may beHearing impairment is a heterogeneous condition with over 40 loci described. Non syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

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Description

The homeobox A1 may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development

the ZIM2 and PEG3 genes do not share exons

resulting in downregulation of cell activation

This gene encodes a small GTP-binding protein of the RAS superfamily which functions as an ADP-ribosylation factor (ARF)

is a frequent finding in alveolar rhabdomyosarcoma

DFNA5 Polyclonal Antibody, 50ul Variant Libraries The homeobox A1 may beHearing impairment is a heterogeneous condition with over 40 loci described. Non syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

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