Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I
Keywords: پاسخ شنوایی مغز ساقه; WS1; Waardenburg syndrome type 1; PAX3; Paired box gene 3; NCC; Neural crest cells; MITF; The Microphthalmia-Associated Transcription Factor; WS3; Waardenburg syndrome type 3; HRCT; The high-resolution computed tomography; MRI; Magnetic resonance imaging;