Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness von Bech-Hansen, N.Torben, Naylor, Margaret J, Maybaum, Tracy A, Sparkes, Rebecca L, Koop, Ben, Birch, David G, Bergen, Arthur A.B, Prinsen, Clemens F.M, Polomeno, Robert C, Gal, Andreas, Drack, Arlene V, Musarella, Maria A, Jacobson, Samuel G, Young, Rockefeller S.L, Weleber, Richard G

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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness von Bech-Hansen, N. Torben, Naylor, Margaret J., Maybaum, Tracy A., Pearce, William G., Koop, Ben, Fishman, Gerald A., Mets, Marilyn, Musarella, Maria A., Boycott, Kym M.

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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants von BOYCOTT, Kym M, MAYBAUM, Tracy A, NAYLOR, Margaret J, WELEBER, Richard G, ROBITAILLE, Johane, MIYAKE, Yozo, BERGEN, Arthur A. B, PIERPONT, Mary Ella, PEARCE, William G, BECH-HANSEN, N. Torben

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Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness von Boycott, Kym M., Pearce, William G., Musarella, Maria A., Weleber, Richard G., Maybaum, Tracy A., Birch, David G., Miyake, Yozo, Young, Rockefeller S.L., Bech-Hansen, N. Torben

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B cells selected for apoptosis in the sheep ileal Peyer's patch have enhanced mutational diversity in the Ig V lambda light chain von Maybaum, TA, Reynolds, JD

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Loss-of-function mutations in a calcium-channel α 1 -subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness von Mets, Marilyn, Maybaum, Tracy A, Pearce, William G, Musarella, Maria A, Naylor, Margaret J, Bech-Hansen, N. Torben, Boycott, Kym M, Fishman, Gerald A, Koop, Ben

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