A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss. - Peng LT; Wang WQ; Huang SS; Liu M; Yang SY; Kang DY; Wang X; Gao X; Yuan YY; Xu JC (Journal of clinical laboratory analysis, 2026)