Relationship between SP1 polymorphism and osteoporosis in β-thalassemia major patients

Pediatrics International

Volumn 50, Issue 4, 2008, Pages 474-476

  Guzeloglu Kayisli, Ozlem ^a   Cetin, Zafer ^a   Keser, Ibrahim ^a   Ozturk, Zeynep ^a   Tuncer, Tiraje ^a   Canatan, Duran ^b   Luleci, Guven ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

^b Thalassemia Center of the State Hospital   (Turkey)

Author keywords

thalassemia major; Collagen type I A1; Osteoporosis; Polymerase chain reaction restriction fragment length polymorphism; Sp1 polymorphism

Indexed keywords

BETA GLOBIN; GUANINE; THYMINE; TRANSCRIPTION FACTOR SP1;

ADOLESCENT; ALLELE; ARTICLE; BINDING SITE; BONE DENSITY; CLINICAL ARTICLE; COLIA1 GENE; CONTROLLED STUDY; FEMALE; GENE; GENETIC POLYMORPHISM; GENOTYPE; HEREDITY; HUMAN; MALE; NUCLEIC ACID BASE SUBSTITUTION; OSTEOPENIA; OSTEOPOROSIS; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; SCHOOL CHILD; THALASSEMIA MAJOR; TURKEY (REPUBLIC);

ADOLESCENT; ADULT; BETA-THALASSEMIA; COLLAGEN TYPE I; FEMALE; HUMANS; MALE; OSTEOPOROSIS; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 50249172828     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2008.02609.x     Document Type: Article

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