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A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
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CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

Roy Morello1, Terry K Bertin, Yuqing Chen

  • 1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

Cell
|October 24, 2006
PubMed

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