Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

✍ Scribed by Cabral, Wayne A; Chang, Weizhong; Barnes, Aileen M; Weis, MaryAnn; Scott, Melissa A; Leikin, Sergey; Makareeva, Elena; Kuznetsova, Natalia V; Rosenbaum, Kenneth N; Tifft, Cynthia J

• Book ID: 109919512
• Publisher: Nature Publishing Group
• Year: 2007
• Tongue: English
• Weight: 545 KB
• Volume: 39
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng1968