Browsing by Subject "CTL"

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Griscelli syndrome: Characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene

Bizario, JCS; Feldmann, J.; Castro, F. A.; Menasche, G.; Jacob, CMA; Cristofani, L.; Casella, E. B.; Voltarelli, J. C.; De Saint-Basile, G.; Espreafico, E. M. (Kluwer Academic/plenum Publ, 2004-07-01)

Griscelli syndrome (GS) is caused by mutations in the MYO5A (GS1), RAB27A (GS2), or MLPH (GS3) genes, all of which lead to a similar pigmentary dilution. in addition, GS1 patients show primary neurological impairment, ...