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In Vivo Lens Deficiency of the R49C αA-Crystallin Mutant
The R49C mutation of αA-crystallin (αA-R49C) causes hereditary cataracts in humans; patients in a four-generation Caucasian family were found be heterozygous for this autosomal dominant mutation. We previously generated knock-in mouse models of this mutation and found that by 2 months of age, hetero...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2873126/ https://ncbi.nlm.nih.gov/pubmed/20188090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2010.02.009 |
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