Haplotypes for 43 VWD animals. Description: Haplotype phases that were estimated using 1009 SNPs on bovine chromosome 22 for two calves with EB, 14 parents of affected calves and 27 control animals of
Clinical and genetic information of an individual with RVOT-VT and a KCNK2 (TREK1) gene mutation obtained after whole exome sequencing.EGA dataset EGAD00001003328
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an autosomal recessive tubular disorder characterized by excessive renal magnesium and calcium excretion and chronic kidney failure.
