Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q-Reference-Cited by-同舟云学术

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

Published:1993-05 Issue:1 Volume:4 Page:54-58
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Jordan Siobhán A.,Farrar G. Jane,Kenna Paul,Humphries Marian M.,Sheils Denise M.,Kumar-Singh Rajendra,Sharp Elizabeth M.,Soriano Nuria,Ayuso Carmen,Benitez Javier,Humphries Peter

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0593-54.pdf

Reference36 articles.

1. Heckenlively, J.R. in Retinitis Pigmentosa 125–1490 (Lippincott, Philadelphia, 1988).

2. Massof, R.W. & Finkelstein, D. Two forms of autosomal dominant retinitis pigmentosa. Doc. Ophthalmol. 51, 28–346 (1981).

3. Lyness, A.L. et al. A clinical, psychophysical and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. Br. J. Ophthalmol. 69, 326–339 (1985).

4. Ott, J. et al. Localisation of multiple retinitis pigmentosa loci on the X chromosome. Proc. natn. Acad. Sci. U.S.A. 87, 701–704 (1990).

5. McWilliam, P. et al. Autosomal dominant retinitis pigmentosa (ADRP): localisation of an ADRP gene to the long arm of chromosome 3. Genomics 5, 619–622 (1989).

Cited by 133 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The New Era of Therapeutic Strategies for the Management of Retinitis Pigmentosa: A Narrative Review of the Pathomolecular Mechanism for Gene Therapies;Cureus;2024-08-13

2. Retinitis Pigmentosa: From Pathomolecular Mechanisms to Therapeutic Strategies;Medicina;2024-01-22

3. Novel Variant IMPDH1 c.134A>G, p.(Tyr45Cys): Phenotype–Genotype Correlation Revealed Likely Benign Clinical Significance;International Journal of Molecular Sciences;2023-07-25

4. Inborn Errors of Purine Salvage and Catabolism;Metabolites;2023-06-24

5. IMPDH1 -associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search;Ophthalmic Genetics;2023-05-31