Linking genotypes with phenotypes in human retinal degenerations: Implications for future research and treatment

Autor:	Michael W. Kaplan
Rok vydání:	1995
Předmět:	Genetics Programmed cell death Blindness Physiology Retinal Biology medicine.disease Phenotype Photoreceptor cell Behavioral Neuroscience chemistry.chemical_compound Neuropsychology and Physiological Psychology medicine.anatomical_structure chemistry Genotype medicine Gene
Zdroj:	Behavioral and Brain Sciences. 18:478-479
ISSN:	1469-1825 0140-525X
DOI:	10.1017/s0140525x00039340
Popis:	Although undoubtedly it will be incomplete by the time it is published, the target article by Daiger et al. organizes mutations in genes that produce retinal degenerations in humans into categories of clinically relevant phenotypes. Such classifications should help us understand the link between altered photoreceptor cell proteins and subsequent cell death, and they may yield insight into methods for preventing consequent blindness.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d164c05683ae002ee1c09710f3abfa40 https://doi.org/10.1017/s0140525x00039340 Zobrazit plný text záznamu