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352337a0
352337a0
https://scigraph.springernature.com/pub.10.1038/352337a0
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
P2888
Q55671357-053F72B5-18AF-4CE5-B79C-D9D8444974FF
P2888
352337a0
https://scigraph.springernature.com/pub.10.1038/352337a0