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A silent mutation in human alpha-A crystallin gene in patients with age-related nuclear or cortical cataract
A cataract is a complex multifactorial disease that results from alterations in the cellular architecture, i.e. lens proteins. Genes associated with the development of lens include crystallin genes. Although crystallins are highly conserved proteins among vertebrates, a significant number of polymor...
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| Publicat a: | Bosn J Basic Med Sci |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5474104/ https://ncbi.nlm.nih.gov/pubmed/28146420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17305/bjbms.2017.1745 |
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