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Lauri B. Hahn

Massachusetts Eye and Ear Infirmary

11

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Missense mutation in the gene encoding the α subunit of rod transducin cosegregates with Nougaret's congenital night blindness

1996 Investigative Ophthalmology & Visual Science
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Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness

1996 Nature Genetics
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Norrie Disease: Diagnosis of a Simplex Case by DNA Analysis

1996 Archives of Ophthalmology
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Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation

1995 Investigative Ophthalmology & Visual Science
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Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa

1994 Investigative Ophthalmology & Visual Science
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Citations (27)
Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1991 Proceedings of the National Academy of Sciences of the United States of America
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Citations (334)
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1991 Nature
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The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA ☆

1991 Genomics
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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

1990 Nature
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Citations (890)