Molecular basis of a progressive juvenile-onset hereditary cataract

In a recent paper, patients with a progressive juvenile-onset hereditary cataract have been reported to have a point mutation in the human γD crystallin gene (Stephan, D. A., Gillanders, E., Vanderveen, D., Freas-Lutz, D., Wistow, G., Baxevanis, A. D., Robbins, C. M., VanAuken, A., Quesenberry, M. I...

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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Pande, Ajay, Pande, Jayanti, Asherie, Neer, Lomakin, Aleksey, Ogun, Olutayo, King, Jonathan A., Lubsen, Nicolette H., Walton, David, Benedek, George B.
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 2000
Matèries:	Biological Sciences
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC15742/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10688888/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.040554397
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