Molecular deletion analysis in Duchenne muscular dystrophy.

Study of 165 unrelated patients with X linked muscular dystrophy (117 with Duchenne and 48 with Becker dystrophy) has shown nine Duchenne cases (8% of the total) where a molecular deletion was detected using probes pERT87 or XJ1.1. No cytogenetic abnormalities were detectable in this unselected seri...

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Main Authors: Thomas, N S, Ray, P N, Worton, R G, Harper, P S
Format: Artigo
Jezik:Inglês
Izdano: 1986
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049831/
https://ncbi.nlm.nih.gov/pubmed/2879923
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