DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L, Claverie-Martin F.
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations.
BMC Med Genet 2019;
20 (01) 6
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