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Photopigment genes, cones, and color update: disrupting the splicing code causes a diverse array of vision disorders

The human long- and middle-wavelength sensitive cone opsin genes exhibit an extraordinary degree of haplotype diversity that results from recombination mechanisms that have intermixed the genes. As a first step in expression, genes—including the protein coding exons and intervening introns—are trans...

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Dettagli Bibliografici
Pubblicato in:Curr Opin Behav Sci
Autori principali: Neitz, Maureen, Patterson, Sara S., Neitz, Jay
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7081934/
https://ncbi.nlm.nih.gov/pubmed/32195292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cobeha.2019.05.004
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