The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson disease [3]

Journal of Medical Genetics

Volumn 36, Issue 2, 1999, Pages 174-

  Ivanova Smolenskaya, I A ^a   Ovchinnikov, I V ^a   Karabanov, A V ^a   Deineko, N L ^a   Poleshchuk, V V ^a   Markova, E D ^a   Illarioshkin, S N ^a  

^a RESEARCH CENTER OF NEUROLOGY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CERULOPLASMIN; COPPER;

AMINO ACID SUBSTITUTION; CLINICAL ARTICLE; HUMAN; LETTER; PRIORITY JOURNAL; RUSSIAN FEDERATION; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CHROMOSOMES, HUMAN, PAIR 13; HEPATOLENTICULAR DEGENERATION; HUMANS; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RUSSIA;

EID: 0033033261     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (8)