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Classic Lattice Corneal Dystrophy Associated with Monoclonal Gammopathy Following Exclusion of a TGFBI Mutation

PURPOSE: To report the association of phenotypic features characteristic of lattice corneal dystrophy with a monoclonal gammopathy of undetermined significance following exclusion of a coding region mutation in TGFBI. DESIGN: Case report METHODS: Slit lamp examination was performed, as well as colle...

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Detalhes bibliográficos
Main Authors: Kamal, Khairidzan M., Rayner, Sylvia A., Chen, Michael C., Aldave, Anthony J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2784604/
https://ncbi.nlm.nih.gov/pubmed/19092416
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICO.0b013e31818200f4
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