C. Griscelli, A syndrome associating partial albinism and immunodeficiency, Am. J. Med, vol.65, pp.691-702, 1978.

C. Klein, Partial albinism with immunodeficiency (Griscelli syndrome), J. Pediatr, vol.125, pp.886-895, 1994.

H. Hurvitz, R. Gillis, S. Klaus, F. Gross-kieselstein, and E. Okon, A kindred with Griscelli disease: spectrum of neurological involvment, Eur. J. Pediatr, vol.152, pp.402-405, 1993.

B. R. Elejalde, Mutations affecting pigmentation in man: I. neuroectodermal melanolysosomal disease, Am. J. Med. Genet, vol.3, pp.65-80, 1979.

E. Pastural, Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene, Nature Genet, vol.16, pp.289-292, 1997.

E. Pastural, Two genes are responsible for Griscelli syndrome at the same 15q21 locus, Genomics, vol.63, pp.299-306, 2000.

T. Tolmachova, Cloning, mapping and characterization of the human RAB27A gene, Gene, vol.239, pp.109-116, 1999.

D. Chen, J. Guo, T. Miki, M. Tachibana, and W. Gahl, Molecular cloning and characterization of Rab27a and Rab27b, novel human rab proteins shared by melanocytes and platelets, Biochem. Mol. Med, vol.60, pp.27-37, 1997.

S. R. Pfeffer, Rab GTPases: master regulators of membrane trafficking, Curr. Opin. Cell Biol, vol.6, pp.522-526, 1994.

P. Novick and M. Zerial, The diversity of Rab proteins in vesicle transport, Curr. Opin. Cell Biol, vol.9, pp.496-504, 1997.

B. Kinsella and W. Maltese, GTP-binding proteins with three different carboxylterminal cysteine motifs are modified in vivo by 20-carbon isoprenoids, J. Biol. Chem, vol.267, pp.3940-3945, 1992.

P. Chavrier and B. Goud, The role of ARF and Rab GTPases in membrane transport, Curr. Opin. Cell Biol, vol.11, pp.466-475, 1999.

S. Stepp, Perforin gene defects in familial hemophagocytic lymphohistiocytosis, Science, vol.286, pp.1957-1959, 1999.

F. J. Barrat, Defective CTLA-4 cycling pathway in Chediak-Higashi syndrome: a possible mechanism for deregulation of T lymphocyte activation, Proc. Natl Acad. Sci. USA, vol.96, pp.8645-8650, 1999.

R. E. Cheney, Brain myosin-V is a two-headed unconventional myosin with motor activity, Cell, vol.75, pp.13-23, 1993.

E. M. Espreafico, Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains, J. Cell Biol, vol.119, pp.1541-1557, 1992.

R. Prekeris and D. M. Terrian, Brain myosin V is a synaptic vesicle-associated motor protein: evidence for a Ca 2+ -dependent interaction with the synaptobrevinsynaptophysin complex, J. Cell Biol, vol.137, pp.1589-1601, 1997.

A. Echard, Interaction of a Golgi-associated kinesin-like protein with Rab6, Science, vol.279, pp.580-585, 1998.

M. C. Seabra, Y. K. Ho, and J. S. Anant, Deficient geranylgeranylation of Ram/Rab27 in choroideremia, J. Biol. Chem, vol.270, pp.24420-24427, 1995.

J. C. Stinchcombe and G. M. Griffiths, Regulated secretion from hemopoietic cells, J. Cell Biol, vol.147, pp.1-5, 1999.

R. Dufourcq-lagelouse, Genetic basis of hemophagocytic lymphohistiocytosis syndrome, Int. J. Mol. Med, vol.4, pp.127-133, 1999.

F. Mazerolles and A. Fischer, Binding of CD4 ligands induces tyrosine phosphorylation of phosphatidinylinositol-3 kinase p110 subunit, Int. Immunol, vol.10, pp.1897-1905, 1998.

S. Kim and W. M. Yokoyama, NK cell granule exocytosis and cytokine production inhibited by Ly-49A engagement, Cell. Immunol, vol.183, pp.10-112, 1998.