MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patients. Li W, Guo L, Chen B, Shu Y, et al. Int J Pediatr Otorhinolaryngol 2023;171:111635.

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Li W, Guo L, Chen B, Shu Y, et al. MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patients. Int J Pediatr Otorhinolaryngol 2023;171:111635.
PMID: 37390746