A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy

Background: The molecular basis of Meesmann's epithelial corneal dystrophy (MECD) has recently been attributed to mutations in the cornea specific keratin genes KRT3 and KRT12. The mechanisms by which these mutations cause the Meesmann's phenotype are not clear. This study presents new dat...

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Detalhes bibliográficos
Main Authors: Irvine, A D, Coleman, C M, Moore, J E, Swensson, O, Morgan, S J, McCarthy, J H, Smith, F J D, Black, G C M, McLean, W H I
Formato: Artigo
Idioma:Inglês
Publicado em: Copyright 2002 British Journal of Ophthalmology 2002
Assuntos:
Scientific Correspondence
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1771195/
https://ncbi.nlm.nih.gov/pubmed/12084738
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