about
A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomalyProfound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL.Prostaglandins in the eye: Function, expression, and roles in glaucoma.FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.Molecular genetics of achromatopsia in Newfoundland reveal genetic heterogeneity, founder effects and the first cases of Jalili syndrome in North America.The interactions of genes, age, and environment in glaucoma pathogenesis.A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect.FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
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description
onderzoeker
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researcher
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հետազոտող
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name
Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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Lance Doucette
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P106
P31
P496
0000-0002-8495-9723