Cita APA

Woo, H., Park, H., Baek, J., Park, M., Kim, U., Sagong, B., & Koo, S. K. (2013). Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. BioMed Central.

Chicago Style Citation

Woo, Hae-Mi, Hong-Joon Park, Jeong-In Baek, Mi-Hyun Park, Un-Kyung Kim, Borum Sagong, i Soo Kyung Koo. Whole-exome Sequencing Identifies MYO15A Mutations As a Cause of Autosomal Recessive Nonsyndromic Hearing Loss in Korean Families. BioMed Central, 2013.

Cita MLA

Woo, Hae-Mi, et al. Whole-exome Sequencing Identifies MYO15A Mutations As a Cause of Autosomal Recessive Nonsyndromic Hearing Loss in Korean Families. BioMed Central, 2013.