Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus

PURPOSE: To evaluate mutations in the visual system homeobox gene 1 (VSX1) and superoxide dismutase 1 (SOD1) genes with keratoconus (KTCN), direct sequencing was performed in an Iranian population. METHODS: One hundred and twelve autosomal dominant KTCN patients and fifty-two unaffected individuals...

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Hlavní autoři: Saee-Rad, Samira, Hashemi, Hassan, Miraftab, Mohammad, Noori-Daloii, Mohammad Reza, Chaleshtori, Morteza Hashemzadeh, Raoofian, Reza, Jafari, Fatemeh, Greene, Wayne, Fakhraie, Ghasem, Rezvan, Farhad, Heidari, Mansour
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Vision 2011
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3235532/
https://ncbi.nlm.nih.gov/pubmed/22171159
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