Old Web
English
Sign In
Acemap
>
authorDetail
>
Qianqian Pang
Qianqian Pang
Shanxi Medical University
Missense mutation
Population
Mutation
Endocrinology
Internal medicine
4
Papers
56
Citations
0.00
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (4)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients
2016
Osteoporosis International
Qianqian Pang
Y. Chi
Zhen Zhao
Xiaoping Xing
Mei Li
Ou Wang
Yan Jiang
R. Liao
Yue Sun
Jin Dong
Weibo Xia
Show All
Source
Cite
Save
Citations (16)
First Report of a Novel Missense CLDN19 Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family
2015
Calcified Tissue International
Tao Yuan
Qianqian Pang
Xiaoping Xing
Xi Wang
Yuhui Li
Jingjun Li
Xueyan Wu
Mei Li
Ou Wang
Yan Jiang
Jin Dong
Weibo Xia
Show All
Source
Cite
Save
Citations (7)
Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families
2015
Metabolic Brain Disease
Qianqian Pang
Xuan Qi
Yan Jiang
Ou Wang
Mei Li
Xiaoping Xing
Jin Dong
Weibo Xia
Show All
Source
Cite
Save
Citations (9)
A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy
2015
Calcified Tissue International
Lu Yuan
Ling Chen
Ruo-xi Liao
Yuan-yuan Lin
Yan Jiang
Ou Wang
Mei Li
Xiaoping Xing
Qianqian Pang
Ruizhi Jiajue
Weibo Xia
Show All
Source
Cite
Save
Citations (24)
1