Cite
HARVARD Citation
Cheng, J. et al. (n.d.). Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family. Annals of human genetics. pp. 410-423. [Online].
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Cheng, J. et al. (n.d.). Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family. Annals of human genetics. pp. 410-423. [Online].