Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutasePeter Huppke, Jutta Gärtner, Cornelia Brendel et al.|Human Mutation|2012Cited by 38
9th International workshop on Fragile X syndrome and X-linked mental retardationJean‐Pierre Fryns, Stephen T. Warren, Andr� Hanauer et al.|American Journal of Medical Genetics|2000Cited by 9
Collaborative prospective study of the fragile X syndrome: One‐year progress reportS. L. Sherman, T. Webb, Gotthold Barbi et al.|American Journal of Medical Genetics|1992Cited by 8