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Michael J. Denton

University of Otago

37

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Ophthalmic Genetics in India: From Tentative Beginnings in the 1980’s to Major Achievements in the Twenty-First Century

2019
- Govindasamy Kumaramanickavel
- Michael J. Denton
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Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan

2008 Clinical Genetics
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Non-allelic mutations in X-linked retinitis pigmentosa

2008 Clinical Genetics
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Physical law not natural selection as the major determinant of biological complexity in the subcellular realm: new support for the pre-Darwinian conception of evolution by natural law

2003 BioSystems
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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

2000 Human Molecular Genetics
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Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination

1998 Human Mutation
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Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3

1998 Genomics
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Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa.

1997 Nature Genetics
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Oguchi Disease, Retinitis Pigmentosa, and the Phototransduction Pathway

1997
- Marion A. Maw
- Michael J. Denton
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Linkage of Blepharophimosis Syndrome in a Large Indian Pedigree to Chromosome 7p

1996 Human Molecular Genetics
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Citations (42)