The ADAMTS(L) family and human genetic disorders

Human Molecular Genetics

Volumn 20, Issue R2, 2011, Pages 163-167

  Le Goff, Carine ^a   Cormier Daire, Valérie ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADAM10 ENDOPEPTIDASE; ADAMTS1 PROTEIN; VON WILLEBRAND FACTOR CLEAVING PROTEINASE; ADAM PROTEIN;

A DISINTEGRIN AND METALLOPROTEINASE WITH THROMBOSPONDIN MOTIFS 17 GENE; A DISINTEGRIN AND METALLOPROTEINASE WITH THROMBOSPONDIN MOTIFS 2 GENE; ADAMTSL2 GENE; ADAMTSL4 GENE; ARTICLE; DYSPLASIA; ECTOPIA LENTIS; EHLERS DANLOS SYNDROME; ENZYME ACTIVITY; EXTRACELLULAR MATRIX; GENE; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; HUMAN; MULTIGENE FAMILY; PRIORITY JOURNAL; PROTEIN FAMILY; THROMBOTIC THROMBOCYTOPENIC PURPURA; WEILL MARCHESANI SYNDROME; ANIMAL; ENZYMOLOGY; GENETICS; METABOLISM; REVIEW;

ADAM PROTEINS; ANIMALS; GENETIC DISEASES, INBORN; HUMANS; MULTIGENE FAMILY;

EID: 84856050942     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddr361     Document Type: Article

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