Cite
HARVARD Citation
Shin, D. et al. (2019). A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Human mutation. 40 (3), pp. 335-346. [Online].
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Shin, D. et al. (2019). A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Human mutation. 40 (3), pp. 335-346. [Online].