John T Gray

Self-complementary adeno-associated virus vectors containing a novel liver-specific human factor IX expression cassette enable highly efficient transduction of murine and nonhuman primate liver.

Geoffrey Kemball-Cook, Jenny McIntosh, Yunyu Spence, 2006, Blood.

Developments in the treatment of hemophilia B: focus on emerging gene therapy

Amit C Nathwani, J. Gray, A. Davidoff, 2013, The Application of Clinical Genetics.

Adenovirus-associated virus vector-mediated gene transfer in hemophilia B.

Pratima Chowdary, Savita Rangarajan, Cecilia Rosales, 2011, The New England journal of medicine.