A Multi-Center Study to Map Genes for Fuchs’ Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability

PURPOSE: To describe the methods for family and case-control recruitment for a multi-center genetic and associated heritability analysis of Fuchs’ Endothelial Corneal Dystrophy (FECD). METHODS: Twenty-nine enrolling sites with 62 trained investigators and coordinators gathered individual and family...

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Bibliografiska uppgifter
Huvudupphovsmän: Louttit, Megan D, Kopplin, Laura J, Igo, Robert P, Fondran, Jeremy R, Tagliaferri, Angela, Bardenstein, David, Aldave, Anthony J, Croasdale, Christopher R, Price, Marianne, Rosenwasser, George O, Lass, Jonathan H, Iyengar, Sudha K
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2012
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3719980/
https://ncbi.nlm.nih.gov/pubmed/22045388
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICO.0b013e31821c9b8f
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