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Fig. 2 | BMC Ophthalmology

Fig. 2

From: Inherited FGFR2 mutation in a Chinese patient with Crouzon syndrome and luxation of bulbus oculi provoked by trauma: a case report

Fig. 2

Identification of mutations in the family. a Sequencing chromatograms of the heterozygous missense mutation (c.1012G > C, p.G338R) in exon 10 of the FGFR2 (upper) and the wild-type sequence (below). b Amino acid sequence of FGFR2 around G338R in a family with Crouzon syndrome, which is a highly conserved segment of the FGFR2 protein in humans and other species. c Molecular modelling of the wild-type and mutant FGFR2 protein

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BMC Ophthalmology

ISSN: 1471-2415

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