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Quaternary structural parameters of the congenital cataract causing mutants of αA-crystallin
Pediatric cataract of the congenital type is the most common form of childhood blindness and it is clinically and genetically heterogeneous. Mutations in 22 different genes have been identified to be associated with congenital cataracts, and among them, eight mutants belong to αA-crystallin. To expl...
Tallennettuna:
| Päätekijät: | , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3788686/ https://ncbi.nlm.nih.gov/pubmed/22045060 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11010-011-1131-8 |
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