For citations:
Barashkov N.A., Vychuzhina L.S., Solovyev A.V., Teryutin F.M., Pshennikova V.G., Burtseva T.E., Tomsky M.I., Platonov F.A., Romanov G.P., Gotovtsev N.N., Dzhemileva L.U., Khusnutdinova E.K., Posukh O.L., Fedorova S.A. Reconstruction of the founder haplotype with mutation c.1621C>T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic (Yakutia). Medical Genetics. 2018;17(8):13-19. (In Russ.) https://doi.org/10.25557/2073-7998.2018.08.13-19
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