More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A.

导出 LinkOut

翻译打印收藏纠错

作者： Caroline,Caetano da Silva ^[1] ; Manon,Ricquebourg ^[1] ; Philippe,Orcel ^[2] ; Stéphanie,Fabre ^[1] ; Thomas,Funck-Brentano ^[2] ; Martine,Cohen-Solal ^[1] ; Corinne,Collet ^[2]

作者单位： Inserm U1132 and Université de Paris, Paris, France. ^[1] Department of Rheumatology, Hôpital Lariboisière, AP-HP, Paris, France. ^[2] Functional Unit of Molecular Biology, Hôpital Lariboisière, AP-HP, Paris, France. ^[3]

关键词 DKK1 LRP5 WNT3A Wnt signaling pathway osteoporosis

主题词青少年(Adolescent);成年人(Adult);发病年龄(Age of Onset);女(雌)性(Female);人类(Humans);胞间信号肽类和蛋白质类(Intercellular Signaling Peptides and Proteins);男(雄)性(Male);中年人(Middle Aged);骨质疏松(Osteoporosis);表型(Phenotype)

DOI 10.1002/mgg3.1681

PMID 33939331

发布时间 2022-01-31

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

Molecular genetics & genomic medicine

2021年9卷6期

e1681页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A.

Molecular genetics & genomic medicine

相似文献

Molecular genetics & genomic medicine

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A.

Molecular genetics & genomic medicine

相似文献

Molecular genetics & genomic medicine

相关期刊

检索历史清除