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Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.

Jing MaXiuli MaKen LinRui HuangXianyun BiCheng MingLi LiXia LiGuo LiLiping ZhaoTao YangYingqin GaoTiesong Zhang
Published in: Human genomics (2023)
The common mutation genes and loci detected in this study were different from those detected in other regions or ethnic groups, which suggested that genetic screening or testing programs for deafness should be formulated in accordance with the genetic characteristics of the region.
Keyphrases
  • genome wide
  • copy number
  • dna methylation
  • hearing loss
  • bioinformatics analysis