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Fig. 3 | BMC Pediatrics

Fig. 3

From: A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum

Fig. 3

The location and phenotypic heterogeneity of amino acid substitutions in the FBN1 protein associated with neonatal Marfan syndrome, and the number of such substitutions in patients with MFS based on the UMD-FBN1 mutations database. nMFS, neonatal Marfan syndrome; iMFS, infantile Marfan syndrome; cMFS, classic Marfan syndrome; icMFS, incomplete Marfan syndrome

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BMC Pediatrics

ISSN: 1471-2431

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