Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C>T mutation in CLCN7.
Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C>T mutation in CLCN7.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@en
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@nl
type
label
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@en
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@nl
prefLabel
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@en
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@nl
P2093
P2860
P356
P1433
P1476
Enhanced but hypofunctional os ...... a c.1856C>T mutation in CLCN7.
@en
P2093
Chunyu Wang
Janet Hock
Xiang Chen
P2860
P2888
P356
10.1038/BONERES.2016.35
P50
P577
2016-11-29T00:00:00Z
P6179
1047186332