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