Novel mutations of CHST6 in Iranian patients with macular corneal dystrophy

PURPOSE: To characterize mutations within the carbohydrate sulfotransferase 6 (CHST6) gene in Iranian subjects from 12 families with macular corneal dystrophy (MCD). METHODS: Genomic DNA was extracted from peripheral blood of 20 affected patients and 60 healthy volunteers followed by polymerase chai...

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Detalles Bibliográficos
Autores principales: Birgani, Shiva Akbari, Salehi, Zivar, Houshmand, Masoud, Mohamadi, Mohamad Javad, Promehr, Leila Azizade, Mozafarzadeh, Zahra
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642847/
https://www.ncbi.nlm.nih.gov/pubmed/19223992

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642847/
https://www.ncbi.nlm.nih.gov/pubmed/19223992

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