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HARVARD Citation
Devlin, L. et al. (2023). Biallelic variants in CEP164 cause a motile ciliopathy‐like syndrome. Clinical genetics. 103 (3), pp. 330-334. [Online].
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Devlin, L. et al. (2023). Biallelic variants in CEP164 cause a motile ciliopathy‐like syndrome. Clinical genetics. 103 (3), pp. 330-334. [Online].