Human cytomegalovirus-infected cells have unstable assembly of major histocompatibility complex class I complexes and are resistant to lysis by cytotoxic T lymphocytes.

Por Warren, A P, Ducroq, D H, Lehner, P J, Borysiewicz, L K
Publicado em 1994

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.

Por Cabot, A, Rozet, J M, Gerber, S, Perrault, I, Ducroq, D, Smahi, A, Souied, E, Munnich, A, Kaplan, J
Publicado em 1999

A third locus for dominant optic atrophy on chromosome 22q

Por Barbet, F, Hakiki, S, Orssaud, C, Gerber, S, Perrault, I, Hanein, S, Ducroq, D, Dufier, J, Munnich, A, Kaplan, J, Rozet, J
Publicado em 2005

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evide...

Por Rozet, J., Gerber, S., Ghazi, I., Perrault, I., Ducroq, D., Souied, E., Cabot, A., Dufier, J., Munnich, A., Kaplan, J.
Publicado em 1999

Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.

Por Perrault, I, Rozet, J M, Ghazi, I, Leowski, C, Bonnemaison, M, Gerber, S, Ducroq, D, Cabot, A, Souied, E, Dufier, J L, Munnich, A, Kaplan, J
Publicado em 1999