Xu, Xiao-Jie <br/><br/>
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.  [electronic resource] 

 -  Journal of human genetics  Feb 2017 
 - 205-211 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1435-232X 
<br/><br/><label>Standard No.: </label>10.1038/jhg.2016.109  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Asian People--genetics<br/>Base Sequence<br/>Bone Density--drug effects<br/>Bone Density Conservation Agents--therapeutic use<br/>Bone Resorption--prevention & control<br/>Child<br/>Child, Preschool<br/>China--epidemiology<br/>Collagen Type I--genetics<br/>Collagen Type I, alpha 1 Chain<br/>Diphosphonates--therapeutic use<br/>Female<br/>Fractures, Bone--drug therapy<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Imidazoles--therapeutic use<br/>Male<br/>Membrane Proteins--genetics<br/>Osteogenesis Imperfecta--drug therapy<br/>Sequence Analysis, DNA<br/>Tacrolimus Binding Proteins--genetics<br/>Young Adult<br/>Zoledronic Acid