Title : Distal renal tubular acidosis: a hereditary disease with an inadequate urinary H⁺ excretion.

Pub. Date : 2013

PMID : 23640117






1 Functional Relationships(s)
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1 Autosomal recessive dRTA is associated with mutations in genes ATP6V1B1, ATP6V0A4 and SLC4A1, which encode subunits a4 and B1 of V-ATPase and the AE1 bicarbonate/chloride exchanger respectively. Bicarbonates solute carrier family 4 member 1 (Diego blood group) Homo sapiens