Exclusion of Four Candidate Genes, <i>KHDRBS2, PTP4A1, KIAA1411</i> and <i>OGFRL1,</i> as Causative of Autosomal Recessive Retinitis Pigmentosa-Reference-Cited by-同舟云学术

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

Published:2005-12-12 Issue:1 Volume:38 Page:19-23
ISSN:0030-3747
Container-title:Ophthalmic Research
language:en
Short-container-title:Ophthalmic Res

Author:

Abd El-Aziz Mai M.,Patel Reshma J.,El-Ashry Mohamed F.,Barragan Isabel,Marcos Irene,Borrego Salud,Antiñolo Guillermo,Bhattacharya Shomi S.

Publisher

S. Karger AG

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology,General Medicine

Reference16 articles.

1. A Major Locus for Autosomal Recessive Retinitis Pigmentosa on 6q, Determined by Homozygosity Mapping of Chromosomal Regions That Contain Gamma-Aminobutyric Acid–Receptor Clusters

2. Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin

3. Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa (RP25)

4. Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus

5. Cloning, characterization, and chromosome mapping of the human GlcAT-S gene

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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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