Mapping, cloning and genetic characterization of the region containing the wilson disease gene

Nature Genetics

Volumn 5, Issue 4, 1993, Pages 338-343

  Petrukhin, K ^a,b   Fischer, S G ^a   Pirastu, M ^c   Tanzi, R E ^d   Chernov, I ^a,b   Devoto, M ^a,b   Brzustowicz, L M ^a,b   Cayanis, E ^a   Vitale, E ^a,b   Russo, J J ^a   Matseoane, D ^a,b   Boukhgalter, B ^a   Wasco, W ^d   Figus, A L ^c   Loudianos, J ^c   Cao, A ^c   Sternlieb, I ^e,f,g   Evgrafov, O ^h   Parano, E ⁱ   Pavone, L ⁱ   Warburton, D ^a   Ott, J ^a,b   Penchaszadeh, G K ^a,b   Scheinberg, I H ^e,f,g   Gilliam, T C ^a,b   more..

^a Department of Psychiatry ^*  (United States)

^b NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

^c Department of Biochemistry and Molecular Biophysics ^*  (Italy)

^d HARVARD MEDICAL SCHOOL   (United States)

^e Howard Hughes Medical Institute   (United States)

^f Natl Ctr Stud of Wilson's Dis   (United States)

^g ST LUKE S ROOSEVELT HOSPITAL CENTER   (United States)

^h RESEARCH CENTRE FOR MEDICAL GENETICS   (Russian Federation)

ⁱ UNIVERSITY OF CATANIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 13Q; GENE ISOLATION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; HAPLOTYPE; HUMAN; MOLECULAR CLONING; WILSON DISEASE;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 13; COMPARATIVE STUDY; COSMIDS; FAMILY; FEMALE; GENETIC MARKERS; GENOMIC LIBRARY; GENOTYPE; HAPLOTYPES; HEPATOLENTICULAR DEGENERATION; HUMAN; LINKAGE DISEQUILIBRIUM; MALE; MOLECULAR SEQUENCE DATA; MUTATION; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027427695     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1293-338     Document Type: Article

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