File:Images of congenital hereditary cataracts due to mutations of crystallin genes.png

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Revision as of 18:57, 16 September 2012 by Z3331330 (talk | contribs)
Images_of_congenital_hereditary_cataracts_due_to_mutations_of_crystallin_genes.png(594 × 190 pixels, file size: 118 KB, MIME type: image/png)

Slit-lamp photographs of the eye of the proband. Slit lamp photographs of the eye of the proband (III:3). A: Front view of the eye of the proband, showing cataract phenotype. B: Slit lamp view of the len of the proband. Lens opacities were mainly located in the nuclear area of lenses as well as in the embryonal and fetal areas.

Images of congenital hereditary cataracts from crystallin mutations[1] Copyright notice This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

reference

  1. Chen, Q, Ma,J,Yan,M,Mothobi,ME, Liu,Y, Zheng, F, A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family 2009 Mol Vis, vol:15,pp.1359–1365.[1]

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current18:48, 16 September 2012Thumbnail for version as of 18:48, 16 September 2012594 × 190 (118 KB)Z3331330 (talk | contribs)Slit-lamp photographs of the eye of the proband. Slit lamp photographs of the eye of the proband (III:3). A: Front view of the eye of the proband, showing cataract phenotype. B: Slit lamp view of the len of the proband. Lens opacities were mainly located
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