Use of sequence variation in three highly variable regions of the mitochondrial DNA for the discrimination of allogeneic platelets

Transfusion

Volumn 46, Issue 4, 2006, Pages 554-561

  Warner, Jessica B ^b   Bruin, Elinda J ^b   Hannig, Horst ^b   Hellenkamp, Frank ^b   Hörning, André ^b   Mittmann, Karin ^b   Van Der Steege, Gerrit ^b   De Leij, Lou F M H ^b   Garritsen, Henk S P ^a  

^a KLINIKUM BRAUNSCHWEIG   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; BLOOD DONOR; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; GENE AMPLIFICATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; NORMAL HUMAN; PROBABILITY; THROMBOCYTE;

BASE SEQUENCE; COMPLEMENTARITY DETERMINING REGIONS; DNA PRIMERS; DNA, MITOCHONDRIAL; HUMANS; PLATELET TRANSFUSION; PROBABILITY; TRANSPLANTATION, HOMOLOGOUS; VARIATION (GENETICS);

EID: 33645275749     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2006.00775.x     Document Type: Article

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