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Girisha, K. et al. (2016). A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy. Clinical genetics. 90 (6), pp. 536-539. [Online].
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Girisha, K. et al. (2016). A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy. Clinical genetics. 90 (6), pp. 536-539. [Online].