Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation

Author:

Lines Matthew A,Hébert Marc,McTaggart Kerry E,Flynn Sarah J,Tennant Matthew T,MacDonald Ian M

Publisher

Elsevier BV

Subject

Ophthalmology

Reference49 articles.

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2. Isolation and nucleotide sequence of the gene encoding human rhodopsin;Nathans;Proc Natl Acad Sci U S A,1984

3. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa;Dryja;N Engl J Med,1990

4. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa;Dryja;Nature,1990

5. Autosomal dominant retinitis pigmentosa;Farrar;Genomics,1990

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