Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths.

Por Bergstrom, R A, You, Y, Erway, L C, Lyon, M F, Schimenti, J C
Publicado em 1998

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Por Heckenlively, J R, Chang, B, Erway, L C, Peng, C, Hawes, N L, Hageman, G S, Roderick, T H
Publicado em 1995

A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.

Por Alagramam, K N, Kwon, H Y, Cacheiro, N L, Stubbs, L, Wright, C G, Erway, L C, Woychik, R P
Publicado em 1999

Enzyme replacement therapy for murine mucopolysaccharidosis type VII leads to improvements in behavior and auditory function.

Por O'Connor, L H, Erway, L C, Vogler, C A, Sly, W S, Nicholes, A, Grubb, J, Holmberg, S W, Levy, B, Sands, M S
Publicado em 1998