Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Nature Genetics

Volumn 38, Issue 4, 2006, Pages 452-457

  Coucke, Paul J ^a   Willaert, Andy ^a   Wessels, Marja W ^b   Callewaert, Bert ^a   Zoppi, Nicoletta ^c   De Backer, Julie ^a   Fox, Joyce E ^d   Mancini, Grazia M S ^b   Kambouris, Marios ^e   Gardella, Rita ^c   Facchetti, Fabio ^c   Willems, Patrick J ^f   Forsyth, Ramses ^g   Dietz, Harry C ^h   Barlati, Sergio ^c   Colombi, Marina ^c   Loeys, Bart ^a   De Paepe, Anne ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF BRESCIA   (Italy)

^d NORTH SHORE UNIVERSITY HOSPITAL   (United States)

^e YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f Genetic Diagnostics Belgium   (Belgium)

^g GHENT UNIVERSITY   (Belgium)

^h JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE TRANSPORTER; GLUCOSE TRANSPORTER 10; PROTEIN; SLC2A10 PROTEIN; TRANSFORMING GROWTH FACTOR BETA; UNCLASSIFIED DRUG;

ANGIOGENESIS; AORTA ANEURYSM; ARTERIAL TORTUOSITY SYNDROME; ARTERY WALL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONTROLLED STUDY; DISEASE ASSOCIATION; FAMILIAL DISEASE; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; HUMAN; HUMAN CELL; HUMAN TISSUE; LOEYS DIETZ SYNDROME; MORPHOGENESIS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; UPREGULATION;

AMINO ACID SEQUENCE; ARTERIES; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; GLUCOSE TRANSPORT PROTEINS, FACILITATIVE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NEOVASCULARIZATION, PATHOLOGIC; PEDIGREE; SEQUENCE HOMOLOGY, AMINO ACID; VASCULAR DISEASES;

EID: 33645381280     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1764     Document Type: Article

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