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

Background and Objectives: The defects in the CLDN16 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’s coding region and can impact on intracellular...

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Detalles Bibliográficos
Autores principales: Rouka, Erasmia, Liakopoulos, Vassilios, Gourgoulianis, Konstantinos I., Hatzoglou, Chrissi, Zarogiannis, Sotirios G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723856/
https://www.ncbi.nlm.nih.gov/pubmed/31357502
http://dx.doi.org/10.3390/medicina55080409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723856/
https://www.ncbi.nlm.nih.gov/pubmed/31357502
http://dx.doi.org/10.3390/medicina55080409

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