|
XB-GENEPAGE-995167
Papers associated with clcn7
???pagination.result.count???
???pagination.result.page??? 1
Sort Newest To Oldest | Sort Oldest To Newest |
Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis., Lee CL, Chang YW, Lin HY, Lee HC, Yeh TC, Fang LC, Lee NC, Tsai JD, Lin SP., Mol Genet Genomic Med. July 1, 2024; 12 (7): e2494. |
|
Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification., Nicoli ER, Weston MR, Hackbarth M, Becerril A, Larson A, Zein WM, Baker PR, Burke JD, Dorward H, Davids M, Huang Y, Adams DR, Zerfas PM, Chen D, Markello TC, Toro C, Wood T, Elliott G, Vu M, Undiagnosed Diseases Network, Zheng W, Garrett LJ, Tifft CJ, Gahl WA, Day-Salvatore DL, Mindell JA, Malicdan MCV., Am J Hum Genet. June 6, 2019; 104 (6): 1127-1138. |
|
A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A, Stauber T, Coppieters W, Ludwig CF, Fasquelle C, Druet T, Zhang Z, Ahariz N, Cambisano N, Jentsch TJ, Charlier C., Dis Model Mech. January 1, 2014; 7 (1): 119-28. |
|
Common gating of both CLC transporter subunits underlies voltage-dependent activation of the 2Cl-/1H+ exchanger ClC-7/Ostm1., Ludwig CF, Ullrich F, Leisle L, Stauber T, Jentsch TJ., J Biol Chem. October 4, 2013; 288 (40): 28611-9. |
???pagination.result.page??? 1