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Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

Published in: Proceedings of the National Academy of Sciences of the United States of America

Date of publication: October 15, 1991

Language: English

Main subject: patient, retinitis pigmentosa, dominant gene

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Cites articles 16

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Spontaneous mutation in man
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Molecular basis of base substitution hotspots in Escherichia coli
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Population genetic studies of retinitis pigmentosa
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Distribution of UV light-induced damage in a defined sequence of human DNA: detection of alkaline-sensitive lesions at pyrimidine nucleoside-cytidine sequences
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Photoproduct frequency is not the major determinant of UV base substitution hot spots or cold spots in human cells
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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
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Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
January 1991

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa
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Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine,Ocular Findings in Patients with Autosomal Dominant Retinitis Pigmentosa and Rhodopsin, Proline-347-Leucine
January 1, 1991

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

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