Genetics in Medicine Open (Jan 2023)

P142: Whole-exome analyses of non-syndromic hearing loss patients from India reveal a wide spectrum of known and novel mutations*

  • Sudipta Chakraborty,
  • Sukanya Mitra,
  • Shamita Sanga,
  • Arnab Ghosh,
  • Suchandra Mukherjee,
  • Nidhan Biswas,
  • Moulinath Acharya

Journal volume & issue
Vol. 1, no. 1
p. 100171

Abstract

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