Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

Genomic DNA from a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia was investigated using cDNA probes for the Duchenne muscular dystrophy (DMD) locus. Genomic probes had not detected a deletion in this patient. Southern analysis of Hind III-digested ge...

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Detalhes bibliográficos
Main Authors: McCabe, E R, Towbin, J, Chamberlain, J, Baumbach, L, Witkowski, J, van Ommen, G J, Koenig, M, Kunkel, L M, Seltzer, W K
Formato: Artigo
Idioma:Inglês
Publicado em: 1989
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC303648/
https://ncbi.nlm.nih.gov/pubmed/2536049
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