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Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort.

Amjad KhanShirui HanRongrong WangMuhammad AnsarWasim AhmadXue Zhang
Published in: Molecular genetics & genomic medicine (2019)
We described common and novel variants in 15 genes in a Pakistani cohort of NSHL.
Keyphrases
  • copy number
  • genome wide
  • hearing loss
  • bioinformatics analysis
  • genome wide identification
  • genome wide analysis
  • dna methylation
  • amino acid