Table 2

Results of FBN1 analysis in 11 consecutive patients affected by predominant EL

PatientMutation siteNucleotideAmino acidProtein domainReferences
OPExon 4C364TR122CEGF-like No 213, 18, 19, this report
BMExon 5A491GN164SEGF-like No 3This report
RWTExon 6C718TR240CHybrid Motif No 113, 14, this report
GBExon 13C1633TR545CcbEGF-like No 413, 17, this report
JLExon 13C1633TR545CcbEGF-like No 413, 17, this report
NSExon 15T1900CS634PcbEGF-like No 6This report
MGExon 15G1955AC652YcbEGF-like No 6This report
VWExon 31A3963GcbEGF-like No 121, this report
IBPIntron 6IVS6 del T -26cbEGF-like No 4022, this report
MZIntron 62IVS62 A+8 to CcbEGF-like No 4114, this report
SRNo mutation identified