成骨不全症,类型Xxiii,也被称为OI23。与成骨不全症,类型Xxiii相关的基因是PHLDB1(Pleckstrin Homology Like Domain Family B Member 1)。相关组织包括骨。
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Osteogenesis Imperfecta, Type Xxiii, is also known as oi23. An important gene associated with Osteogenesis Imperfecta, Type Xxiii is PHLDB1 (Pleckstrin Homology Like Domain Family B Member 1). Affiliated tissues include bone.