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- W2003325423 endingPage "151" @default.
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- W2003325423 abstract "Exceptional progress has been made during the past two decades in identifying genes causing inherited retinal diseases such as retinitis pigmentosa. An inescapable consequence is that the relationship between genes, mutations, and clinical findings has become very complex. Success in identifying the causes of inherited retinal diseases has many implications, including a better understanding of the biological basis of vision and insights into the processes involved in retinal pathology. From a clinical point of view, there are two important questions arising from these developments: where do we stand today in finding disease-causing mutations in affected individuals, and what are the implications of this information for clinical practice? This perspective addresses these questions specifically for retinitis pigmentosa, but the observations apply generally to other forms of inherited eye disease." @default.
- W2003325423 created "2016-06-24" @default.
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- W2003325423 date "2007-02-01" @default.
- W2003325423 modified "2023-10-17" @default.
- W2003325423 title "Perspective on Genes and Mutations Causing Retinitis Pigmentosa" @default.
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- W2003325423 doi "https://doi.org/10.1001/archopht.125.2.151" @default.
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