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
Zdroj: Gene Therapy. Jan2014, Vol. 21 Issue 1, p96-105. 10p.
Databáze: Academic Search Ultimate