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Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
Sung CH, Davenport CM, Hennessey JC, Maumenee IH, Jacobson SG, Heckenlively JR, Nowakowski R, Fishman G, Gouras P, Nathans J. Sung CH, et al. Among authors: nathans j. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6481-5. doi: 10.1073/pnas.88.15.6481. Proc Natl Acad Sci U S A. 1991. PMID: 1862076 Free PMC article.
Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain.
Sung CH, Davenport CM, Nathans J. Sung CH, et al. Among authors: nathans j. J Biol Chem. 1993 Dec 15;268(35):26645-9. J Biol Chem. 1993. PMID: 8253795 Free article.
-H., Schneider, B., Agarwal, N., Papermaster, D.S., and Nathans, J. (1991) Proc. Natl. Acad. Sci. U.S.A. 88, 8840-8844), these experiments define distinct classes of biochemical defects in human rhodopsin and further show that amino acid substitutions in class II re …
-H., Schneider, B., Agarwal, N., Papermaster, D.S., and Nathans, J. (1991) Proc. Natl. Acad. Sci. U.S.A. 88, 8840-8844), these …
Molecular genetics of human visual pigments.
Nathans J, Merbs SL, Sung CH, Weitz CJ, Wang Y. Nathans J, et al. Annu Rev Genet. 1992;26:403-24. doi: 10.1146/annurev.ge.26.120192.002155. Annu Rev Genet. 1992. PMID: 1482119 Review. No abstract available.
216 results