The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
Rudolph E. Tanzi(Harvard University), T. Conrad Gilliam(Institut thématique Génétique, génomique et bioinformatique), Jean‐Luc Pellequer, Donna Romano(Harvard University), Linda M. Brzustowicz(Rutgers, The State University of New Jersey), Wilma Wasco(Harvard University), Barry Honig(Columbia University), Ashley I. Bush(Florey Institute of Neuroscience and Mental Health), Enrico Parano(University of Catania), James F. Gusella(Broad Institute), Mario Pirastu(Institute of History of Mediterranean Europe), И. П. Чернов(Institute of Bioorganic Chemistry), Oleg V. Evgrafov(State University of New York), Irmin Sternlieb(New School), I. Herbert Scheinberg(New School), Marcella Devoto(Children's Hospital of Philadelphia), Graciela K. Penchaszadeh(New York State Psychiatric Institute), Piero Pavone(University of Catania), B. Ross(New York State Psychiatric Institute), I. S. Edelman(Reproductive Medicine Associates of New York), Konstantin Petrukhin(Cleveland Clinic Lerner College of Medicine), MA Soares(New York State Psychiatric Institute), Jeffrey Peppercorn(Stem Cell Institute)
Cited by 1,381
Related Papers
Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease
|Neurology|1993|3.8k
The <i>GPR54</i> Gene as a Regulator of Puberty
|New England Journal of Medicine|2003|2.5k
A polymorphic DNA marker genetically linked to Huntington's disease
|Nature|1983|2.3k
Association between Microdeletion and Microduplication at 16p11.2 and Autism
|New England Journal of Medicine|2008|1.7k