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Publikováno v:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 32(6)
Osteogenesis imperfecta (OI) is characterized by bone fragility and increased fracture susceptibility. BMP1 variants have been reported in the rare OI type XIII, specifically referred to herein as BMP1-associated autosomal recessive (AR) OI. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15c7cceba7d569dc0bdd24b0e4cd3574
https://pubmed.ncbi.nlm.nih.gov/33624138
https://pubmed.ncbi.nlm.nih.gov/33624138
