Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency

Thrombosis and Haemostasis

Volumn 108, Issue 1, 2012, Pages 94-100

  Lind Halldén, Christina ^a   Dahlén, Anna ^b   Hillarp, Andreas ^c   Zöller, Bengt ^b   Dahlbäck, Björn ^c   Halldén, Christer ^a  

^a KRISTIANSTAD UNIVERSITY   (Sweden)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

^c LUND UNIVERSITY   (Sweden)

Author keywords

Familial thrombosis; Molecular biology methods; Protein C S pathway; Thrombophilia; Venous thrombosis

Indexed keywords

PROTEIN S;

ARTICLE; CHROMOSOME 3; CONTROLLED STUDY; DNA SEQUENCE; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; HAPLOTYPE; HUMAN; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; MUTATIONAL ANALYSIS; POINT MUTATION; PRIORITY JOURNAL; PROS1 GENE; PROTEIN S DEFICIENCY;

BLOOD PROTEINS; CYTOGENETIC ANALYSIS; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MULTIPLEX POLYMERASE CHAIN REACTION; PEDIGREE; POINT MUTATION; PROTEIN S DEFICIENCY; SEQUENCE DELETION; SWEDEN;

EID: 84863645771     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH12-01-0040     Document Type: Article

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