Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele-Reference-Cited by-同舟云学术

Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele

Published:1997-11 Issue:5 Volume:61 Page:1059-1066
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

McGee T.L.,Devoto M.,Ott J.,Berson E.L.,Dryja T.P.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference39 articles.

1. Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19;Al-Maghtheh;Hum Mol Genet,1994

2. Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11), and association with a unique bimodal expressivity phenotype;Al-Maghtheh;Am J Hum Genet,1996

3. An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q;Bardien;Hum Mol Genet,1995

4. Dominant retinitis pigmentosa with reduced penetrance;Berson;Arch Ophthalmol,1969

5. Dominant retinitis pigmentosa with reduced penetrance: further studies of the electroretinogram;Berson;Arch Ophthalmol,1979

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