Works matching AU Gardner, Leigh M.

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 15, p. 2405, doi. 10.1093/hmg/ddn140

By:

• Jacobson, Samuel G.;
• Cideciyan, Artur V.;
• Aleman, Tomas S.;
• Sumaroka, Alexander;
• Roman, Alejandro J.;
• Gardner, Leigh M.;
• Prosser, Haydn M.;
• Mishra, Monalisa;
• Bech-Hansen, N. Torben;
• Herrera, Waldo;
• Schwartz, Sharon B.;
• Liu, Xue-Zhong;
• Kimberling, William J.;
• Steel, Karen P.;
• Williams, David S.

Publication type:

Article