A carregar...
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...
Na minha lista:
| Publicado no: | Bosn J Basic Med Sci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
2017
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|