Four novel mutations of the PKD2 gene in Czech families with autosomal dominant polycystic kidney disease.

Human mutation

Volumn 19, Issue 5, 2002, Pages 573-

  Reiterova J ^a   Stekrova J ^a   Peters, D J ^a   Kapras, J ^a   Kohoutova M ^a   Merta, M ^a   Zidovska J ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; POLYCYSTIN; POLYCYSTIN 2;

ARTICLE; CZECH REPUBLIC; FAMILY; FRAMESHIFT MUTATION; GENETIC POLYMORPHISM; GENETICS; HETERODUPLEX ANALYSIS; HUMAN; KIDNEY POLYCYSTIC DISEASE; METHODOLOGY; MISSENSE MUTATION; MUTATION; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON;

CODON, NONSENSE; CZECH REPUBLIC; FAMILY; FRAMESHIFT MUTATION; HETERODUPLEX ANALYSIS; HUMANS; MEMBRANE PROTEINS; MUTATION; MUTATION, MISSENSE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; TRPP CATION CHANNELS;

EID: 19244368286     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9035     Document Type: Article

References (0)