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Development of a CRISPR/Cas9-mediated gene editing platform to restore the reading frame for 60% of Duchenne muscular dystrophy patients |
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Titel: |
Development of a CRISPR/Cas9-mediated gene editing platform to restore the reading frame for 60% of Duchenne muscular dystrophy patients |
Auteur: |
Young, C. Hicks, M. Ermolova, N. Nakano, H. Jan, M. Younesi, S. Nelson, S. Miceli, C. Pyle, A. Spencer, M. |
Verschenen in: |
Neuromuscular disorders |
Paginering: |
Jaargang 26 (2016) nr. S2 pagina's 2 p. |
Jaar: |
2016 |
Inhoud: |
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Uitgever: |
Published by Elsevier B.V. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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