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TMEM38B gene

Known as: D4Ertd89e, TRANSMEMBRANE PROTEIN 38B, TRIC-B 
National Institutes of Health

Papers overview

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2017
2017
Context Recessive mutations in TMEM38B cause type XIV osteogenesis imperfecta (OI) by dysregulating intracellular calcium flux… 
2016
2016
Recessive osteogenesis imperfecta (OI) is caused by defects in proteins involved in post-translational interactions with type I… 
Review
2013
Review
2013
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and deformity and growth deficiency… 
Highly Cited
2013
Highly Cited
2013
Autosomal recessive osteogenesis imperfecta (OI) was diagnosed in three unrelated Israeli Bedouin consanguineous families… 
Highly Cited
2012
Highly Cited
2012
Background Osteogenesis imperfecta (OI) is an hereditary bone disease in which increased bone fragility leads to frequent…