Molecular therapy of primary hyperoxaluria
Author:
Funder
Secretaría de Estado de Investigación, Desarrollo e Innovación
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1007/s10545-017-0045-3/fulltext.html
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4. Castello R, Borzone R, D’Aria S, Annunziata P, Piccolo P, Brunetti-Pierri N (2016) Helper-dependent adenoviral vectors for liver-directed gene therapy of primary hyperoxaluria type 1. Gene Ther 23:129–134
5. Cellini B, Montioli R, Paiardini A, Lorenzetto A, Voltattorni CB (2009) Molecular insight into the synergism between the minor allele of human liver Peroxisomal alanine:Glyoxylate aminotransferase and the F152I mutation. J Biol Chem 284:8349–8358
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