Large-scale Molecular Analysis of a 34 Mb Interval on Chromosome 6q: Major Refinement of the RP25 Interval-Reference-Cited by-同舟云学术

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Large-scale Molecular Analysis of a 34 Mb Interval on Chromosome 6q: Major Refinement of the RP25 Interval

Published:2008-07 Issue:4 Volume:72 Page:463-477
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Ann Human Genet

Author:

Abd El-Aziz M. M.,Barragan I.,O'Driscoll C.,Borrego S.,Abu-Safieh L.,Pieras J. I.,El-Ashry M. F.,Prigmore E.,Carter N.,Antinolo G.,Bhattacharya S. S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2008.00455.x/fullpdf

Reference56 articles.

1. Molecular Genetic Analysis of Two Functional Candidate Genes in the Autosomal Recessive Retinitis Pigmentosa, RP25, Locus

2. Exclusion of Four Candidate Genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as Causative of Autosomal Recessive Retinitis Pigmentosa

3. Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

4. The Spectrum of SLC17A5-Gene Mutations Resulting in Free Sialic Acid–Storage Diseases Indicates Some Genotype-Phenotype Correlation

Cited by 7 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. Large-scale Molecular Analysis of a 34 Mb Interval on Chromosome 6q: Major Refinement of the RP25 Interval;Annals of Human Genetics;2014-12-22

2. Identification and Analysis of Inherited Retinal Disease Genes;Methods in Molecular Biology;2012

3. Novel Null Mutations in theEYSGene Are a Frequent Cause of Autosomal Recessive Retinitis Pigmentosa in the Israeli Population;Investigative Opthalmology & Visual Science;2010-09-01

4. Current World Literature;Current Opinion in Ophthalmology;2009-09

5. Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa;The American Journal of Human Genetics;2008-11

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