Cite
HARVARD Citation
Macnamara, E. et al. (2019). Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. Human mutation. 40 (5), pp. 532-538. [Online].
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Macnamara, E. et al. (2019). Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. Human mutation. 40 (5), pp. 532-538. [Online].