A novel claudin-16 mutation, severe bone disease, and nephrocalcinosis

被引:11
作者
Nadarajah, Luxme [1 ]
Khosravi, Maryam [2 ]
Dumitriu, Simona [2 ]
Klootwijk, Enriko [2 ]
Kleta, Robert [2 ]
Yaqoob, Muhammad M. [1 ]
Walsh, Stephen B. [2 ]
机构
[1] Royal London Hosp, Renal Unit, Barts Hlth, London E1 1BB, England
[2] UCL, UCL Ctr Nephrol, London, England
关键词
D O I
10.1016/S0140-6736(13)62673-2
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
[No abstract available]
引用
收藏
页码:98 / 98
页数:1
相关论文
共 5 条
[1]
Disorders of calcium and magnesium balance: a physiology-based approach [J].
Hoorn, Ewout J. ;
Zietse, Robert .
PEDIATRIC NEPHROLOGY, 2013, 28 (08) :1195-1206
[2]
Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex [J].
Hou, Jianghui ;
Renigunta, Aparna ;
Konrad, Martin ;
Gornes, Antonio S. ;
Schneeberger, Eveline E. ;
Paul, David L. ;
Waldegger, Siegfried ;
Goodenough, Daniel A. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (02) :619-628
[3]
PATHOPHYSIOLOGY OF THE RENAL ACIDIFICATION DEFECT PRESENT IN THE SYNDROME OF FAMILIAL HYPOMAGNESEMIA-HYPERCALCIURIA [J].
RODRIGUEZSORIANO, J ;
VALLO, A .
PEDIATRIC NEPHROLOGY, 1994, 8 (04) :431-435
[4]
WRONG O, 1959, Q J MED, V28, P259
[5]
Wrong OM, 2005, OXFORD TEXTBOOK OF C