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Schema
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Lewis, RA
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created
[InstanceEdit:2466812] Jassal, Bijay, 2012-09-12
dbId
2466769
displayName
Lewis, RA
firstname
R A
initial
RA
publications
[LiteratureReference:5605179] Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
[LiteratureReference:2471734] Molecular genetics of human blue cone monochromacy
[LiteratureReference:2471710] Genetic heterogeneity among blue-cone monochromats
[LiteratureReference:5262899] A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations
[LiteratureReference:2466818] A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
schemaClass
Person
surname
Lewis
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