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Malhotra A, Ziegler A, Shu L, et al. De novo missense variants in . J Med Genet. 2020;58(10):712-716doi: 10.1136/jmedgenet-2020-107137.
Malhotra, A., Ziegler, A., Shu, L., Perrier, R., Amlie-Wolf, L., Wohler, E., Lygia de Macena Sobreira, N., Colin, E., Vanderver, A., Sherbini, O., Stouffs, K., Scalais, E., Serretti, A., Barth, M., Navet, B., Rollier, P., Xi, H., Wang, H., Zhang, H., Perry, D. L., Ferrarini, A., Colombo, R., Pepler, A., Schneider, A., Tomiwa, K., Okamoto, N., Matsumoto, N., Miyake, N., Taft, R., Mao, X., & Bonneau, D. (2021). De novo missense variants in . Journal of medical genetics, 58(10), 712-716. https://doi.org/10.1136/jmedgenet-2020-107137
Malhotra, Alka, et al. "De novo missense variants in ." Journal of medical genetics vol. 58,10 (2021): 712-716. doi: https://doi.org/10.1136/jmedgenet-2020-107137
Malhotra A, Ziegler A, Shu L, Perrier R, Amlie-Wolf L, Wohler E, Lygia de Macena Sobreira N, Colin E, Vanderver A, Sherbini O, Stouffs K, Scalais E, Serretti A, Barth M, Navet B, Rollier P, Xi H, Wang H, Zhang H, Perry DL, Ferrarini A, Colombo R, Pepler A, Schneider A, Tomiwa K, Okamoto N, Matsumoto N, Miyake N, Taft R, Mao X, Bonneau D. De novo missense variants in . J Med Genet. 2021 Oct;58(10):712-716. doi: 10.1136/jmedgenet-2020-107137. Epub 2020 Aug 20. PMID: 32820033.
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