Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations

BACKGROUND: Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis type 1 is an autosomal recessive disease characterized by excessive renal magnesium and calcium excretion, bilateral nephrocalcinosis, and progressive chronic renal failure. This rare disease is caused by mutations in CLDN...

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Detalles Bibliográficos
Autores principales: Perdomo-Ramirez, Ana, de Armas-Ortiz, Marian, Ramos-Trujillo, Elena, Suarez-Artiles, Lorena, Claverie-Martin, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325764/
https://www.ncbi.nlm.nih.gov/pubmed/30621608
http://dx.doi.org/10.1186/s12881-018-0713-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325764/
https://www.ncbi.nlm.nih.gov/pubmed/30621608
http://dx.doi.org/10.1186/s12881-018-0713-7

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