A genetic study of Wilson's disease: evidence for heterogeneity.

[1]  D. B. McConnell,et al.  The production of copper 67 from natural zinc using a linear acceleration. , 1970, The International journal of applied radiation and isotopes.

[2]  S. Osborn,et al.  Studies with radioactive copper (64Cu and 67Cu) in relation to the natural history of Wilson's disease. , 1967, Lancet.

[3]  H. Kunkel,et al.  Localization of Cu64 in Serum Fractions Following Oral Administration , 1954, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[4]  N. A. Holtzman,et al.  Identification of an apoceruloplasmin-like substance in the plasma of copper-deficient rats. , 1970, The Journal of biological chemistry.

[5]  G. Gregoriadis,et al.  Role of Protein in Removal of Copper from the Liver , 1968, Nature.

[6]  B. Combes,et al.  DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE. , 1961, The Journal of clinical investigation.

[7]  N Mantel,et al.  A simple method of estimating the segregation ratio under complete ascertainment. , 1968, American journal of human genetics.

[8]  R. Carrico,et al.  Some properties of ceruloplasmin from patients with Wilson's disease☆ , 1969 .

[9]  W. N. Tauxe,et al.  Radiocopper studies in patients with Wilson's disease and their relatives. , 1966, The American journal of medicine.

[10]  D. Cox.  A screening test for Wilson's disease and its application to psychiatric patients. , 1967, Canadian Medical Association journal.

[11]  A. Bearn.  A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration) , 1959, Annals of human genetics.

[12]  J. Walshe,et al.  Studies on the toxicity of copper. II. The behaviour of microsomal membrane ATPase of the pigeon’s brain tissue to copper and some other metallic substances , 1966, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[13]  G. Cropp.  Changes in blood and plasma volumes during growth. , 1971, The Journal of pediatrics.

[14]  Phillips Jn.  Some aspects of metal incorporation into porphyrins. , 1967 .

[15]  I. Sternlieb,et al.  Prevention of Wilson's disease in asymptomatic patients. , 1968, The New England journal of medicine.

[16]  A. Morell,et al.  PHYSICAL AND CHEMICAL STUDIES ON CERULOPLASMIN. 3. A STABILIZING COPPER-COPPER INTERACTION IN CERULOPLASMIN. , 1965, The Journal of biological chemistry.

[17]  D. Cox.  Factors influencing serum ceruloplasmin levels in normal individuals. , 1966, The Journal of laboratory and clinical medicine.

[18]  M E Carruthers,et al.  Raised serum copper and caeruloplasmin levels in subjects taking oral contraceptives , 1966, Journal of clinical pathology.

[19]  E. Frieden,et al.  The mobilization of iron from the perfused mammalian liver by a serum copper enzyme, ferroxidase I. , 1971, The Journal of biological chemistry.

[20]  J. Walshe.  The physiology of copper in man and its relation to Wilson's disease. , 1967, Brain : a journal of neurology.

[21]  N. A. Holtzman,et al.  Studies on the rate of release and turnover of ceruloplasmin and apoceruloplasmin in rat plasma. , 1970, The Journal of biological chemistry.

[22]  J. Soothill,et al.  A family study of the biochemical defects in Wilson's disease , 1961, Journal of clinical pathology.

[23]  W. B. Matthews,et al.  The metabolic disorder in hepato-lenticular degeneration. , 1952, The Quarterly journal of medicine.

[24]  D. Shreffler,et al.  Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function. , 1969, Proceedings of the National Academy of Sciences of the United States of America.

[25]  A. Bearn.  Genetic and biochemical aspects of Wilson's disease. , 1953, The American journal of medicine.

[26]  J. Bush,et al.  Studies on copper metabolism. XIV. Radioactive copper studies in normal subjects and in patients with hepatolenticular degeneration. , 1955, The Journal of clinical investigation.

[27]  S. Sherlock,et al.  Presymptomatic Wilson's disease. , 1967, The Lancet.

[28]  A. Sass-kortsak,et al.  Observations on ceruloplasmin in Wilson's disease. , 1959, The Journal of clinical investigation.

[29]  I. Sternlieb,et al.  The diagnosis of Wilson's disease in asymptomatic patients. , 1963, JAMA.

[30]  L. Broman.  CHROMATOGRAPHIC AND MAGNETIC STUDIES ON HUMAN CERULOPLASMIN. , 1964, Acta Societatis Medicorum Upsaliensis.

[31]  I. Scheinberg,et al.  Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease). , 1952, Science.