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Heterozygous Vitamin D Receptor Gene Polymorphism in an Osteogenesis Imperfecta Type Osteogenesis Imperfecta Type IV Case
Osteogenesis imperfecta (OI) type IV is a clinical entity with autosomal dominant inheritance in type 1 collagen genes; collagen, type I, alpha 2 (COL1A2) and more rarely collagen, type I, alpha 1 (COL1A1) point mutation ...