Cite
HARVARD Citation
Xu, S. et al. (2020). Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection. Molecular genetics & genomic medicine. 8 (1), p. n/a. [Online].
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Xu, S. et al. (2020). Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection. Molecular genetics & genomic medicine. 8 (1), p. n/a. [Online].