Add to ORKGBSND encodes barttin, an accessory subunit of renal and inner ear chloride channels. To date, all mutations of BSND have been shown t
Background. ClC-Ka and ClC-Kb, chloride channels participating in renal tubular Cl transport, requir...
CLC-K/barttin chloride channels are essential for NaCl re-absorption in Henle's loop and for potassi...
Bartter syndrome with sensorineural deafness (type IV Bartter syndrome) is a subtype of this tubular...
Renal salt loss in Bartter's syndrome is caused by impaired transepithelial transport in the loop of...
Antenatal Bartter syndrome (aBS) comprises a heterogeneous group of autosomal recessive salt-losing ...
In the mammalian ear, transduction of sound stimuli is initiated by K+ entry through mechano-sensiti...
BSND encodes barttin, an accessory subunit of renal and inner ear chloride channels. To date, all mu...
Human Bartter syndrome IV is an autosomal recessive disorder characterized by congenital deafness an...
textabstractHuman Bartter syndrome IV is an autosomal recessive disorder characterized by congenital...
Barttin, a gene product of BSND, is one of four genes responsible for Bartter syndrome. Co-expressio...
Type III and IV Bartter syndromes (BS) are rare kidney tubulopathies caused by loss-of-function muta...
Dent disease 1 (DD1) is a renal salt-wasting tubulopathy associated with mutations in the Cl-/H+ ant...
CLC-K chloride channels are expressed in the kidney and in the inner ear and require the accessory s...
ClC-K chloride channels are crucial for auditory transduction and urine concentration. Mutations in ...
Barttin is an accessory subunit of ClC-K chloride channels expressed in the kidney and the inner ear...
Background. ClC-Ka and ClC-Kb, chloride channels participating in renal tubular Cl transport, requir...
CLC-K/barttin chloride channels are essential for NaCl re-absorption in Henle's loop and for potassi...
Bartter syndrome with sensorineural deafness (type IV Bartter syndrome) is a subtype of this tubular...
Renal salt loss in Bartter's syndrome is caused by impaired transepithelial transport in the loop of...
Antenatal Bartter syndrome (aBS) comprises a heterogeneous group of autosomal recessive salt-losing ...
In the mammalian ear, transduction of sound stimuli is initiated by K+ entry through mechano-sensiti...
BSND encodes barttin, an accessory subunit of renal and inner ear chloride channels. To date, all mu...
Human Bartter syndrome IV is an autosomal recessive disorder characterized by congenital deafness an...
textabstractHuman Bartter syndrome IV is an autosomal recessive disorder characterized by congenital...
Barttin, a gene product of BSND, is one of four genes responsible for Bartter syndrome. Co-expressio...
Type III and IV Bartter syndromes (BS) are rare kidney tubulopathies caused by loss-of-function muta...
Dent disease 1 (DD1) is a renal salt-wasting tubulopathy associated with mutations in the Cl-/H+ ant...
CLC-K chloride channels are expressed in the kidney and in the inner ear and require the accessory s...
ClC-K chloride channels are crucial for auditory transduction and urine concentration. Mutations in ...
Barttin is an accessory subunit of ClC-K chloride channels expressed in the kidney and the inner ear...
Background. ClC-Ka and ClC-Kb, chloride channels participating in renal tubular Cl transport, requir...
CLC-K/barttin chloride channels are essential for NaCl re-absorption in Henle's loop and for potassi...
Bartter syndrome with sensorineural deafness (type IV Bartter syndrome) is a subtype of this tubular...