Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

Autor: L M, Kunkel, J F, Hejtmancik, C T, Caskey, A, Speer, A P, Monaco, W, Middlesworth, C A, Colletti, C, Bertelson, U, Müller, M, Bresnan, F, Shapiro, U, Tantravahi, J, Speer, S A, Latt, R, Bartlett, M A, Pericak-Vance, A D, Roses, M W, Thompson, P N, Ray, R G, Worton, K H, Fischbeck, P, Gallano, M, Coulon, C, Duros, J, Boue, C, Junien, J, Chelly, G, Hamard, M, Jeanpierre, M, Lambert, J C, Kaplan, A, Emery, H, Dorkins, S, McGlade, K E, Davies, C, Boehm, B, Arveiler, C, Lemaire, G J, Morgan, M J, Denton, J, Amos, M, Bobrow, F, Benham, E, Boswinkel, C, Cole, V, Dubowitz, K, Hart, S, Hodgson, L, Johnson, A, Walker, L, Roncuzzi, A, Ferlini, C, Nobile, G, Romeo, D E, Wilcox, N A, Affara, M A, Ferguson-Smith, M, Lindolf, H, Kaariainen, A, de la Chapelle, V, Ionasescu, C, Searby, R, Ionasescu, E, Bakker, G J, van Ommen, P L, Pearson, C R, Greenberg, J L, Hamerton, K, Wrogemann, R A, Doherty, R, Polakowska, C, Hyser, S, Quirk, N, Thomas, J F, Harper, B T, Darras, U, Francke

Publikováno v: Nature. 322:73-77

Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemical defect is as yet unknown. Recently, two cloned segments of human X-chromosome DNA have been described which detect structural alterations within or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac42acd99365ac65d56ea50d27b3a3c5
https://doi.org/10.1038/322073a0