Lin, M., Liu, Z., Liu, G., Zhao, S., Li, C., Chen, W., . . . Wu, N. (2019). Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1. Mol Genet Genomic Med.
Citação norma ChicagoLin, Mao, et al. "Genetic and Molecular Mechanism for Distinct Clinical Phenotypes Conveyed By Allelic Truncating Mutations Implicated in FBN1." Mol Genet Genomic Med 2019.
MLA citiranjeLin, Mao, et al. "Genetic and Molecular Mechanism for Distinct Clinical Phenotypes Conveyed By Allelic Truncating Mutations Implicated in FBN1." Mol Genet Genomic Med 2019.
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