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HARVARD Citation
Lin, M. et al. (2020). Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1. Molecular genetics & genomic medicine. 8 (1), p. n/a. [Online].
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Lin, M. et al. (2020). Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1. Molecular genetics & genomic medicine. 8 (1), p. n/a. [Online].