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Problems and solutions in myoblast transfer therapy
Duchenne muscular dystrophy is a severe X‐linked neuromuscular disease that affects approximately 1/3500 live male births in every human population, and is caused by a mutation in the gene that encodes the muscle protein dystrophin. The characterization and cloning of the dystrophin gene in 1987 was...
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| Foilsithe in: | J Cell Mol Med |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Blackwell Publishing Ltd
2007
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6737837/ https://ncbi.nlm.nih.gov/pubmed/12067449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2001.tb00136.x |
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