Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

  • Hae Mi Woo
  • , Hong Joon Park
  • , Jeong In Baek
  • , Mi Hyun Park
  • , Un Kyung Kim
  • , Borum Sagong
  • , Soo Kyung Koo

Research output: Contribution to journal › Article › peer-review

38 Scopus citations

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Biochemistry, Genetics and Molecular Biology