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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