The molecular basis of phenylalanine hydroxylase deficiency in Croatia.

Human mutation

Volumn 21, Issue 4, 2003, Pages 399-

  Zschocke, Johannes ^a   Preusse, Astrid ^a   Sarnavka, Vladimir ^a   Fumic, Ksenija ^a   Mardesic, Dusko ^a   Hoffmann, Georg F ^a   Baric, Ivo ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ARTICLE; CROATIA; ENZYMOLOGY; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETICS; HAPLOTYPE; HUMAN; METHODOLOGY; MUTATION; PHENYLKETONURIA; POPULATION GENETICS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; STATISTICS;

CROATIA; GENETICS, POPULATION; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MUTATION; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0037390448     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9115     Document Type: Article

References (0)