For citations:
Bogorad A.E., Dyakova S.E., Mizernitskiy Yu.L., Sokolova L.V., Zakharov P.P., Zorina I.E., Kostyuchenko M.V., Shatokha P.A. Rare mutation of the CCNO gene in patients with primary ciliary dyskinesia. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2018;63(6):83-87. (In Russ.) https://doi.org/10.21508/1027-4065-2018-63-5-83-87
Email this article 