Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation.
暂无分享，去创建一个
Z. Gai | Yi Liu | Haiyan Zhang | Xiaomeng Yang | Yue Li | Jingyun Guan | Rui Dong | Zilong Li | Guangyu Wang
[1] X. Xing,et al. A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy , 2015, Calcified Tissue International.
[2] F. Yıldız,et al. A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy , 2013, Modern rheumatology.