The spermatogenesis-associated protein-7 (SPATA7) gene – an overview
Author:
Affiliation:
1. Kallam Anji Reddy Molecular Genetics Laboratory, Prof Brien Holden Eye Research Centre, L.V. Prasad Eye Institute, Hyderabad, India
Funder
Hyderabad Eye Research Foundation
Champalimaud Fundation
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2020.1807025
Reference27 articles.
1. A novel gene, RSD-3/HSD-3.1, encodes a meiotic-related protein expressed in rat and human testis
2. A novel locus for Leber congenital amaurosis on chromosome 14q24
3. Mutation Survey of Known LCA Genes and Loci in the Saudi Arabian Population
4. Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa
5. Identification of Novel Mutations in Patients with Leber Congenital Amaurosis and Juvenile RP by Genome-wide Homozygosity Mapping with SNP Microarrays
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1. Spata7 is required for maintenance of the retinal connecting cilium;Scientific Reports;2022-04-02
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