Mutations in COQ8B (ADCK4) found in patients with steroid‐resistant nephrotic syndrome alter COQ8B function

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|39|3|406-414

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.39, Iss.3, 2018-03, pp. : 406-414

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Analysis of HBV genotype, drug resistant mutations, and pre‐core/basal core promoter mutations in Korean patients with acute hepatitis B

By  

JOURNAL OF MEDICAL VIROLOGY, Vol. 87, Iss. 6, 2015-06 ,pp. : 993-998

John Wiley & Sons Inc

Access to resources Recommend Favorite

IL8 and Cathepsin B as Melanoma Serum Biomarkers

By Zhang Hongtao   Fu Ting   McGettigan Suzanne   Kumar Suresh   Liu Shujing   Speicher David   Schuchter Lynn   Xu Xiaowei  

International Journal of Molecular Sciences, Vol. 12, Iss. 3, 2011-02 ,pp. : 1505-1518

MDPI

Access to resources Recommend Favorite

Characterisation of K+ Currents in the C8-B4 Microglial Cell Line and their Regulation by Microglia Activating Stimuli

By  

Cellular Physiology and Biochemistry, Vol. 24, Iss. 3-4, 2009-08 ,pp. : 141-152

Karger

Access to resources Recommend Favorite

Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy

By  

CNS: NEUROSCIENCE AND THERAPEUTICS, Vol. 21, Iss. 8, 2015-08 ,pp. : 626-630

John Wiley & Sons Inc

Access to resources Recommend Favorite

DLL4 loss‐of‐function heterozygous mutations cause Adams–Oliver syndrome

By  

CLINICAL GENETICS, Vol. 88, Iss. 6, 2015-12 ,pp. : 532-532

John Wiley & Sons Inc

Access to resources Recommend Favorite