Male infertility may be associated with IFT140 -related autosomal recessive retinitis pigmentosa
Author:
Affiliation:
1. Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA
2. Genetics, University of Wisconsin Madison – Waisman Center, Madison, Wisconsin, USA
Funder
Research to Prevent Blindness
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2023.2291672
Reference15 articles.
1. Retinitis pigmentosa
2. Intraflagellar Transport Genes Are Essential for Differentiation and Survival of Vertebrate Sensory Neurons
3. Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations
4. Early-onset severe retinal dystrophy as the initial presentation of IFT140-related skeletal ciliopathy
5. Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140
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