Cite
HARVARD Citation
Eisenberger, T. et al. (n.d.). Targeted and Genomewide NGS Data Disqualify Mutations in MYO1A, the "DFNA48 Gene", as a Cause of Deafness. Human mutation. 35 (5), pp. 565-570. [Online].
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Eisenberger, T. et al. (n.d.). Targeted and Genomewide NGS Data Disqualify Mutations in MYO1A, the "DFNA48 Gene", as a Cause of Deafness. Human mutation. 35 (5), pp. 565-570. [Online].