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352337A0
352337A0
http://dx.doi.org/10.1038/352337A0
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
P356
Q55671357-47CD9539-AEEE-4FCB-8272-2456755751EA
P356
352337A0
http://dx.doi.org/10.1038/352337A0