Altered Mitochondrial Function in Type 2 Granular Corneal Dystrophy

Type 2 granular corneal dystrophy (GCD2) is caused by point mutation R124H in the transforming growth factor-β–induced gene (TGFBI) and is characterized by age-dependent progression of corneal deposits. Mitochondrial features in heterozygous GCD2 and normal corneal tissues was evaluated using electr...

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Detalhes bibliográficos
Main Authors: Kim, Tae-im, Kim, Hanna, Lee, Doo Jae, Choi, Seung-Il, Kang, Sang Won, Kim, Eung Kweon
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2011
Assuntos:
Regular Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3157179/
https://ncbi.nlm.nih.gov/pubmed/21699880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2011.04.005
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