Novel mutations of SOX10 gene in Chinese patients with type II Waardenburg syndrome.
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DOI: 10.1016/j.ijporl.2020.110172
Abstract: Waardenburg Syndrome (WS) is a condition characterized by sensorineural deafness and pigment disturbances of the skin, hair and iris. By using the latest genomics technology, the WS-related gene mutations and corresponding mechanisms have been widely… read more here.
Keywords: sox10 gene; novel mutations; waardenburg syndrome; gene chinese ... See more keywords