Faber PW. et al "Huntingtin interacts with a family of WW domain proteins"   Hum Mol Genet. 1998 Sep;7(9):1463-74
Tumer Z. et al "Mutation spectrum of ATP7A, the gene defective in Menkes disease"   Adv Exp Med Biol. 1999;448:83-95
Tanzi RE. et al "The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene"   Nat Genet. 1993 Dec;5(4):344-50
Bull PC. et al "The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene"   Nat Genet. 1993 Dec;5(4):327-37
Troelstra C. et al "ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes"   Cell. 1992 Dec 11;71(6):939-53
Jaspers NG. et al "First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure"   Am J Hum Genet. 2007 Mar;80(3):457-66
Evidente VG. "Is it a tic or Tourette's? Clues for differentiating simple from more complex tic disorders"   Postgrad Med. 2000 Oct;108(5):175-6, 179-82
†The statements on this Web site have not been evaluated by the Food and Drug Administration (FDA). And are not intended to diagnose, treat, cure or prevent disease. The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider. Nothing presented here is intended as a substitute for prescription medication or any other medical treatment prescribed by your doctor.