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deafness, autosomal dominant, /26
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ACTG1
Isolation and characterization of full-length cDNA clones for human alpha-, beta-, and gamma-actin mRNAs: skeletal but not cytoplasmic actins have an amino-terminal cysteine that is subsequently removed
Villin is a major protein of the microvillus cytoskeleton which binds both G and F actin in a calcium-dependent manner
Microtubule associated protein MAP1A is an actin-binding and crosslinking protein
Localization of the calcium-sensitive actin monomer binding site in gelsolin to segment 4 and identification of calcium binding sites
Functional molecular complexes of human N-formyl chemoattractant receptors and actin
Human actin depolymerizing factor mediates a pH-sensitive destruction of actin filaments
GJB3
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
GJB6
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
Cancer Gene Census
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Regulation of actin cytoskeleton
Homo sapiens (human)
one gene
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