Inherited protein S deficiency as a reszult of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification

Journal of Thrombosis and Haemostasis

Volumn 6, Issue 8, 2008, Pages 1430-1432

  Choung, H S ^a   Kim, Hee Jin ^a   Gwak, G Y ^a   Kim, S H ^a   Kim, D K ^a  

^a Sungkyunkwan University School of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN S; PROTEIN S 1;

ADULT; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; GENE AMPLIFICATION; GENE DUPLICATION; GENE REARRANGEMENT; GENE SEQUENCE; GENETIC RISK; HUMAN; LETTER; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; POLYMERASE CHAIN REACTION; PORTAL VEIN THROMBOSIS; PRIORITY JOURNAL; PROTEIN S DEFICIENCY; SEQUENCE ANALYSIS;

ADULT; BASE SEQUENCE; BLOOD PROTEINS; DNA; EXONS; GENE DUPLICATION; GENE REARRANGEMENT; HETEROZYGOTE; HUMANS; MALE; MUTATION; NUCLEIC ACID AMPLIFICATION TECHNIQUES; PORTAL VEIN; PROTEIN S DEFICIENCY; VENOUS THROMBOSIS;

EID: 47649101708     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2008.03026.x     Document Type: Letter

References (13)

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