Cite
HARVARD Citation
Ramzan, M. et al. (2021). Variants of human CLDN9 cause mild to profound hearing loss. Human mutation. 42 (10), pp. 1321-1335. [Online].
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Ramzan, M. et al. (2021). Variants of human CLDN9 cause mild to profound hearing loss. Human mutation. 42 (10), pp. 1321-1335. [Online].