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Langouët M, Siquier-Pernet K, Sanquer S, et al. Contiguous mutation syndrome in the era of high-throughput sequencing. Mol Genet Genomic Med. 2015;3(3):215-20doi: 10.1002/mgg3.134.
Langouët, M., Siquier-Pernet, K., Sanquer, S., Bole-Feysot, C., Nitschke, P., Boddaert, N., Munnich, A., Mancini, G. M., Barouki, R., Amiel, J., & Colleaux, L. (2015). Contiguous mutation syndrome in the era of high-throughput sequencing. Molecular genetics & genomic medicine, 3(3), 215-20. https://doi.org/10.1002/mgg3.134
Langouët, Maéva, et al. "Contiguous mutation syndrome in the era of high-throughput sequencing." Molecular genetics & genomic medicine vol. 3,3 (2015): 215-20. doi: https://doi.org/10.1002/mgg3.134
Langouët M, Siquier-Pernet K, Sanquer S, Bole-Feysot C, Nitschke P, Boddaert N, Munnich A, Mancini GM, Barouki R, Amiel J, Colleaux L. Contiguous mutation syndrome in the era of high-throughput sequencing. Mol Genet Genomic Med. 2015 May;3(3):215-20. doi: 10.1002/mgg3.134. Epub 2015 Mar 18. PMID: 26029708; PMCID: PMC4444163.
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