Dystrophin in frameshift deletion patients with Becker muscular dystrophy.

In a previous study we identified 14 cases with Duchenne muscular dystrophy (DMD) or its milder variant, Becker muscular dystrophy (BMD), with a deletion of exons 3-7, a deletion that would be expected to shift the translational reading frame of the mRNA and give a severe phenotype. We have examined...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Gangopadhyay, S B, Sherratt, T G, Heckmatt, J Z, Dubowitz, V, Miller, G, Shokeir, M, Ray, P N, Strong, P N, Worton, R G
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682710/
https://ncbi.nlm.nih.gov/pubmed/1496988
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items