Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase

American Journal of Human Genetics

Volumn 67, Issue 2, 2000, Pages 295-301

  Irrthum, Alexandre ^a   Karkkainen, Marika J ^b   Devriendt, Koen ^c   Alitalo, Kari ^b   Vikkula, Miikka ^a  

^a DE DUVE INSTITUTE   (Belgium)

^b UNIVERSITY OF HELSINKI   (Finland)

^c UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE KINASE; VASCULOTROPIN RECEPTOR;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOPHOSPHORYLATION; CHROMOSOME 5Q; FEMALE; GENE EXPRESSION; GENE INACTIVATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; HUMAN; MALE; MILROY DISEASE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION;

EID: 0033862310     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303019     Document Type: Article

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