In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria

<i>Background and Objectives:</i> The defects in the <i>CLDN16</i> gene are a cause of primary hypomagnesemia (FHHNC), which is characterized by massive renal magnesium wasting, resulting in nephrocalcinosis and renal failure. The mutations occur throughout the gene&#8217...

Full description

Bibliographic Details

Published in:	Medicina
Main Authors:	Erasmia Rouka, Vassilios Liakopoulos, Konstantinos I. Gourgoulianis, Chrissi Hatzoglou, Sotirios G. Zarogiannis
Format:	Article
Language:	English
Published:	MDPI AG 2019-07-01
Subjects:	bioinformatics CLDN16 FHHNC interactome mitochondria subcellular localization
Online Access:	https://www.mdpi.com/1010-660X/55/8/409