Kategorie:
PubID
Gen
MIM
26963950 Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
AP2S1
PMC3163795 Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects
BSND
PMC3163795 Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects 26963950 Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences. 26323216 Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.
CASR
26946774 Srp Arh Celok Lek. 2015: Pseudo-Bartter's Syndrome in Patients with Cystic Fibrosis
CFTR
PMC3163795 Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects
CLCNKA
25810436 ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
CLCNKB
28674042 A Novel Hypokalemic-Alkalotic Salt-Losing Tubulopathy in Patients with CLDN10 Mutations.
CLDN10
CTNS
26963950 Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences. 23802516 Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia.
GNA11
KCNJ1
27120771 Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
MAGED2
PMC3163795 Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects
SLC12A1
PMC3163795 Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects
SLC12A3