Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.

One hundred and thirty-two Scottish families, representing the majority of currently known cases in this country with at least one living subject affected by DMD (110) or BMD (22), were studied with a series of cDNA probes excluding the 3' region of the gene (probes 10-14). Using mainly HindIII...

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Veröffentlicht in:J Med Genet
Hauptverfasser: Cooke, A, Lanyon, W G, Wilcox, D E, Dornan, E S, Kataki, A, Gillard, E F, McWhinnie, A J, Morris, A, Ferguson-Smith, M A, Connor, J M
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMJ Publishing Group 1990
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017078/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2191136/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.5.292
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