Učitavanje...
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...
Spremljeno u:
| Glavni autori: | , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2010
|
| Teme: | |
| Online pristup: | 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 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|