Lea Bennett to Mutation
This is a "connection" page, showing publications Lea Bennett has written about Mutation.
Connection Strength
2.585
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Expanding the Mutation Spectrum for Inherited Retinal Diseases. Genes (Basel). 2024 Dec 28; 16(1).
Score: 0.731
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Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases. Genes (Basel). 2021 06 29; 12(7).
Score: 0.574
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Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. Ophthalmic Genet. 2021 02; 42(1):15-22.
Score: 0.546
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Examination of VLC-PUFA-deficient photoreceptor terminals. Invest Ophthalmol Vis Sci. 2014 Apr 24; 55(7):4063-72.
Score: 0.349
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Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):19.
Score: 0.154
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Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1). Transl Vis Sci Technol. 2020 04; 9(5):14.
Score: 0.132
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Current Progress in Deciphering Importance of VLC-PUFA in the Retina. Adv Exp Med Biol. 2016; 854:145-51.
Score: 0.098