Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Gaël Ménasché, Élodie Pastural, Jérôme Feldmann et al. · Nature Genetics · 2000 · 952 citations

Life Sciences, Genetics, Molecular Genetics +7

A syndrome associating partial albinism and immunodeficiency

C Griscelli, Anne Durandy, Delphine Guy‐Grand et al. · The American Journal of Medicine · 1978 · 385 citations

Life Sciences, Genetics, Immunology +12

Slac2-a/Melanophilin, the Missing Link between Rab27 and Myosin Va

Mitsunori Fukuda, Taruho S. Kuroda, Katsuhiko Mikoshiba · Journal of Biological Chemistry · 2002 · 360 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +12

A Family of Rab27-binding Proteins

Molly Strom, Alistair N. Hume, Abul K. Tarafder et al. · Journal of Biological Chemistry · 2002 · 322 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +14

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Gaël Ménasché, Chen Hsuan Ho, Özden Sanal et al. · Journal of Clinical Investigation · 2003 · 289 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17