Molecular study of the hydroxymethylbilane synthase gene (HMBS) among Polish patients with acute intermittent porphyria.

Human mutation

Volumn 19, Issue 3, 2002, Pages 310-

  Gregor, Anita ^a   Schneider Yin, Xiaoye ^a   Szlendak, Urszula ^a   Wettstein, Albert ^a   Lipniacka, Agnieszka ^a   Rüfenacht, Urszula B ^a   Minder, Elisabeth I ^a  

^a INSTITUTE OF HEMATOLOGY AND TRANSFUSION MEDICINE   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOLEVULINIC ACID; DIAGNOSTIC AGENT; DNA; PORPHOBILINOGEN DEAMINASE;

ACUTE INTERMITTENT PORPHYRIA; ADULT; ARTICLE; COMPARATIVE STUDY; ENZYME ASSAY; ENZYMOLOGY; FEMALE; GENETIC PROCEDURES; GENETICS; HUMAN; METHODOLOGY; MIDDLE AGED; POLAND; STANDARD; URINE;

ADULT; AMINOLEVULINIC ACID; DNA; ENZYME TESTS; FEMALE; GENETIC TECHNIQUES; HUMANS; HYDROXYMETHYLBILANE SYNTHASE; MIDDLE AGED; POLAND; PORPHYRIA, ACUTE INTERMITTENT;

EID: 19044373028     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: None     Document Type: Article

References (0)