8 results for author:"Hahn L.B." in Literature citations
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| Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa. Dryja T.P., Hahn L.B., Kajiwara K., Berson E.L. Invest. Ophthalmol. Vis. Sci. 38:1972-1982(1997) · UniProtKB (1) |
| Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness. Dryja T.P., Hahn L.B., Reboul T., Arnaud B. |
| Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa. Hahn L.B., Berson E.L., Dryja T.P. Invest. Ophthalmol. Vis. Sci. 35:1077-1082(1994) · UniProtKB (1) |
| Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. Dryja T.P., McGee T.L., Hahn L.B., Cowley G.S., Olsson J.E., Reichel E., Sandberg M.A., Berson E.L. N. Engl. J. Med. 323:1302-1307(1990) · UniProtKB (1) · Mapped (2) |
| A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Dryja T.P., McGee T.L., Reichei E., Hahn L.B., Cowley G.S., Yandell D.W., Sandberg M.A., Berson E.L. Nature 343:364-366(1990) · UniProtKB (1) |
| Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa. Dryja T.P., Hahn L.B., Cowley G.S., McGee T.L., Berson E.L. Proc. Natl. Acad. Sci. U.S.A. 88:9370-9374(1991) · UniProtKB (1) |
| Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Kajiwara K., Hahn L.B., Mukai S., Travis G.H., Berson E.L., Dryja T.P. Nature 354:480-483(1991) · UniProtKB (1) |
| The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA. Travis G.H., Christerson L., Danielson P.E., Klisak I., Sparkes R.S., Hahn L.B., Dryja T.P., Sutcliffe G.J. Genomics 10:733-739(1991) · UniProtKB (1) |