Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts

OBJECTIVE(S): Childhood cataract is a genetically heterogeneous eye disorder that results in visual impairment. The aim of this study was to identify the genetic mutations of connexin 50 gene among Iranian families suffered from autosomal dominant congenital cataracts (ADCC). MATERIALS AND METHODS:...

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Bibliografiset tiedot
Julkaisussa:Iran J Basic Med Sci
Päätekijät: Mohebi, Masoumeh, Chenari, Saeed, Akbari, Abolfazl, Ghassemi, Fariba, Zarei-Ghanavati, Mehran, Fakhraie, Ghasem, Babaie, Nahid, Heidari, Mansour
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Mashhad University of Medical Sciences 2017
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Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5378966/
https://ncbi.nlm.nih.gov/pubmed/28392901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22038/IJBMS.2017.8358
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