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Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model.
PLoS Genet. 2022 Jun 8;18(6):e1009798. doi: 10.1371/journal.pgen.1009798. eCollection 2022 Jun.
PLoS Genet. 2022.
PMID: 35675330
Free PMC article.
Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes.
Gogna N, Weatherly S, Zhao F, Collin GB, Pinkney J, Stone L, Naggert JK, Carter GW, Nishina PM.
Gogna N, et al. Among authors: weatherly s.
Int J Mol Sci. 2022 Jan 30;23(3):1615. doi: 10.3390/ijms23031615.
Int J Mol Sci. 2022.
PMID: 35163536
Free PMC article.
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A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.
Collin GB, Shi L, Yu M, Akturk N, Charette JR, Hyde LF, Weatherly SM, Pera MF, Naggert JK, Peachey NS, Nishina PM, Krebs MP.
Collin GB, et al. Among authors: weatherly sm.
Int J Mol Sci. 2022 Feb 17;23(4):2220. doi: 10.3390/ijms23042220.
Int J Mol Sci. 2022.
PMID: 35216333
Free PMC article.
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