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Bennett, Lea
One or more keywords matched the following items that are connected to
Bennett, Lea
Item Type
Name
Concept
Mutation
Academic Article
Current Progress in Deciphering Importance of VLC-PUFA in the Retina.
Academic Article
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1.
Academic Article
Examination of VLC-PUFA-deficient photoreceptor terminals.
Academic Article
Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1).
Grant
Genotype phenotype associations in inherited retinal degeneration
Grant
Rod photoreceptor function in retinitis pigmentosa
Academic Article
Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases.
Academic Article
Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2.
Search Criteria
Mutation