Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).

Cellular and molecular biology (Noisy-le-Grand, France)

Volumn 47 Online Pub, Issue , 2001, Pages

  Seidel, J ^a   Caca, K ^a   Schwab, S G ^a   Berr, F ^a   Wildenauer, D B ^a   Mentzel, H J ^a   Horn, N ^a   Kauf, E ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CATION TRANSPORT PROTEIN; COPPER; DNA; PENICILLAMINE; WILSON DISEASE PROTEIN; ZINC ACETATE;

ADOLESCENT; ARTICLE; CASE REPORT; EXON; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; MISSENSE MUTATION; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; URINE; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ADOLESCENT; BASE SEQUENCE; CATION TRANSPORT PROTEINS; COPPER; DNA; DNA MUTATIONAL ANALYSIS; EXONS; GENOTYPE; HEPATOLENTICULAR DEGENERATION; HUMANS; MALE; MUTATION; MUTATION, MISSENSE; PENICILLAMINE; PHENOTYPE; ZINC ACETATE;

EID: 0000224473     PISSN: 01455680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)