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Fig. 4 | BMC Medical Genomics

Fig. 4

From: Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families

Fig. 4

Sequence analysis and clinical examination of the family 4: (A) Pedigree of the family 4:The filled black symbol represents the affected member, a central dot denotes carriers, and the arrow denotes the proband. (B) The fundus of both eyes:the retina of both eyes were normal.The macular structure of both eyes was intact and the thickness was normal on OCT. (C) Sequence chromatograms of identified mutations. (D) The homology of amino acid sequences between human FRMD7 and other species. The amino acid at position 626 is highly conserved among species, the mutated residue 626 is boxed and indicated

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BMC Medical Genomics

ISSN: 1755-8794

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