ID-bases-logo
- databases for immunodeficiency-causing variations

   MYO5Abase
   Variation registry for  Griscelli syndrome, type 1 (GS1)


MYO5Abase mutation publications

[1997]

Search PubMed latest citations for MYO5A mutations

    1997

  • Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene.
    Pastural E, Barrat FJ, Dufourcq-Lagelouse R, Certain S, Sanal O, Jabado N, Seger R, Griscelli C, Fischer A, de Saint Basile G
    Nat Genet 1997(3): 289-92 [PubMed abstract].