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Fig. 5 | BMC Medical Genomics

Fig. 5

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

Fig. 5

Sequence analysis and clinical examination of the family 5: (A) Pedigree of the family 5: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:Fundus tessellation with no reflection observed in macular fovea; the macular structure of both eyes was normal for OCT. (C) Sequence chromatograms of identified mutations (D) The homology of amino acid sequences between human HMGB3 and other species. The amino acid at positions 192 and 193 are highly conserved among species, and the mutated residues 192 and 193 are boxed and indicated

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BMC Medical Genomics

ISSN: 1755-8794

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