High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.

Human mutation

Volumn 25, Issue 6, 2005, Pages 595-

  Schulte, Claudia ^a   Geisthoff, Urban ^a   Lux, Andreas ^a   Kupka, Susan ^a   Zenner, Hans Peter ^a   Blin, Nikolaus ^a   Pfister, Markus ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN RECEPTOR 2; ACVRL1 PROTEIN, HUMAN; CELL SURFACE RECEPTOR; ENG PROTEIN, HUMAN; LEUKOCYTE ANTIGEN;

ARTICLE; EXON; GENE FREQUENCY; GENETIC SCREENING; GENETICS; GERMANY; HUMAN; INTRON; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RENDU OSLER WEBER DISEASE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ACTIVIN RECEPTORS, TYPE II; ANTIGENS, CD; DNA MUTATIONAL ANALYSIS; EXONS; GENE FREQUENCY; GENETIC SCREENING; GERMANY; HUMANS; INTRONS; MUTATION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RECEPTORS, CELL SURFACE; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 34548070211     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9345     Document Type: Article

References (0)