Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene

PURPOSE: To evaluate the TGFBI gene and the encoded transforming growth factor beta-induced protein (TGFBIp) in a 47-year-old African-American patient with an unusual atypical asymmetric lattice corneal dystrophy (LCD). METHODS: The eyes of the proband and his brother were examined by slit-lamp biom...

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Autori principali: Afshari, Natalie A., Bahadur, Rosanna P., Eifrig, David E., Thogersen, Ida B., Enghild, Jan J., Klintworth, Gordon K.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Molecular Vision 2008
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2268855/
https://ncbi.nlm.nih.gov/pubmed/18385782
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