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Yigit G, Brown KE, Kayserili H, et al. Mutations in CDK5RAP2 cause Seckel syndrome. Mol Genet Genomic Med. 2015;3(5):467-80doi: 10.1002/mgg3.158.
Yigit, G., Brown, K. E., Kayserili, H., Pohl, E., Caliebe, A., Zahnleiter, D., Rosser, E., Bögershausen, N., Uyguner, Z. O., Altunoglu, U., Nürnberg, G., Nürnberg, P., Rauch, A., Li, Y., Thiel, C. T., & Wollnik, B. (2015). Mutations in CDK5RAP2 cause Seckel syndrome. Molecular genetics & genomic medicine, 3(5), 467-80. https://doi.org/10.1002/mgg3.158
Yigit, Gökhan, et al. "Mutations in CDK5RAP2 cause Seckel syndrome." Molecular genetics & genomic medicine vol. 3,5 (2015): 467-80. doi: https://doi.org/10.1002/mgg3.158
Yigit G, Brown KE, Kayserili H, Pohl E, Caliebe A, Zahnleiter D, Rosser E, Bögershausen N, Uyguner ZO, Altunoglu U, Nürnberg G, Nürnberg P, Rauch A, Li Y, Thiel CT, Wollnik B. Mutations in CDK5RAP2 cause Seckel syndrome. Mol Genet Genomic Med. 2015 Sep;3(5):467-80. doi: 10.1002/mgg3.158. Epub 2015 May 24. PMID: 26436113; PMCID: PMC4585455.
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