Mutation analysis in patients with Wilson disease: identification of 4 novel mutations. Mutation in brief no. 250. Online.

Human mutation

Volumn 14, Issue 1, 1999, Pages 88-

  Haas, R ^a   Gutierrez Rivero, B ^a   Knoche, J ^a   Boker K ^a   Manns, M P ^a   Schmidt, H H ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CARRIER PROTEIN; CATION TRANSPORT PROTEIN; WILSON DISEASE PROTEIN;

ARTICLE; GENETICS; HUMAN; MUTATION; SINGLE STRAND CONFORMATION POLYMORPHISM; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; HEPATOLENTICULAR DEGENERATION; HUMANS; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0032605196     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)14:1<88::AID-HUMU15>3.0.CO;2-H     Document Type: Article

References (0)