DFNA5 Polyclonal Antibody, 100ul Drug Development and Evaluation a disorder characterized by severely

a disorder characterized by severely reduced brain size and mental retardation

which are stem-loop structures found in the 5' UTR of ferritin mRNA

The channel activity is directed by the pore-forming alpha-1 subunit

The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family

Cleavage stimulation factor subunit 2 is a member of the cleavage stimulation factor (CSTF) complex that is involved in the 3' end cleavage and polyadenylation of pre-mRNAs

DFNA5 Polyclonal Antibody, 100ul Drug Development and Evaluation a disorder characterized by severelyHearing 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.