Cite
HARVARD Citation
Kim, B. et al. (2017). Discovery of MYH14 as an important and unique deafness gene causing prelingually severe autosomal dominant nonsyndromic hearing loss. Journal of gene medicine. p. n/a. [Online].
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Kim, B. et al. (2017). Discovery of MYH14 as an important and unique deafness gene causing prelingually severe autosomal dominant nonsyndromic hearing loss. Journal of gene medicine. p. n/a. [Online].