File:Lattice corneal dystrophy type 1.JPEG

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Lattice_corneal_dystrophy_type_1.JPEG ‎(500 × 500 pixels, file size: 71 KB, MIME type: image/jpeg)

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English: Lattice corneal dystrophy type I. A network of thick linear corneal opacities in patient with a variant of LCD1 (LCD type III) due to a homozygous p. Leu527Arg mutation in the TGFBI gene. Klintworth Orphanet Journal of Rare Diseases 2009 4:7 doi:10.1186/1750-1172-4-7
Русский: Решётчатая дистрофия роговицы тип I.
Date
Source Corneal dystrophies
Author Klintworth GK.
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(Reusing this file)		 © 2009 Klintworth; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Date/TimeThumbnailDimensionsUserComment
current08:58, 6 July 2009Thumbnail for version as of 08:58, 6 July 2009500 × 500 (71 KB)CopperKettle (talk | contribs){{Information |Description={{en|1=Lattice corneal dystrophy type I. A network of thick linear corneal opacities in patient with a variant of LCD1 (LCD type III) due to a homozygous p. Leu527Arg mutation in the TGFBI gene. Klintworth Orphanet Journal of Ra
08:58, 6 July 2009No thumbnail500 × 500 (71 KB)CopperKettle (talk | contribs){{Information |Description={{en|1=Lattice corneal dystrophy type I. A network of thick linear corneal opacities in patient with a variant of LCD1 (LCD type III) due to a homozygous p. Leu527Arg mutation in the TGFBI gene. Klintworth Orphanet Journal of Ra

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