Tyrosine capsid-mutant AAV vectors for gene delivery to the canine retina from a subretinal or intravitreal approach.
Autor: | Mowat, F M1, Gornik, K R1, Dinculescu, A2, Boye, S L2, Hauswirth, W W2, Petersen-Jones, S M1, Bartoe, J T1 |
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Zdroj: | Gene Therapy. Jan2014, Vol. 21 Issue 1, p96-105. 10p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |