Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas")

American Journal of Human Genetics

Volumn 70, Issue 4, 2002, Pages 866-874

  Brouillard, Pascal ^a   Boon, Laurence M ^a,b   Mulliken, John B ^c   Enjolras, Odile ^f   Ghassibé, Michella ^a   Warman, Matthew L ^g   Tan, O T ^e   Olsen, Bjorn R ^d   Vikkula, Miikka ^a  

^a DE DUVE INSTITUTE   (Belgium)

^b UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

^c Children s Hospital   (Belgium)

^d HARVARD MEDICAL SCHOOL   (United States)

^e TUFTS UNIVERSITY   (United States)

^f HÔPITAL LARIBOISIÈRE   (France)

^g CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENE PRODUCT; GLOMULIN; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 1P; CONTROLLED STUDY; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENE MUTATION; GLOMUS TUMOR; HUMAN; MAJOR CLINICAL STUDY; MALE; MORPHOGENESIS; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PATHOGENESIS; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STOP CODON; VEIN MALFORMATION;

GLOMUS;

EID: 0036201378     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/339492     Document Type: Article

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