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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1990
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017078/
https://ncbi.nlm.nih.gov/pubmed/2191136
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia