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Citation: An. Smith et al., Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing, NAT GENET, 26(1), 2000, pp. 71-75

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Citation: Fe. Karet et al., Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness, NAT GENET, 21(1), 1999, pp. 84-90

Authors: Karet, FE Finberg, KE Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Medina, JF Lifton, RP

Citation: Fe. Karet et al., Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34, AM J HU GEN, 65(6), 1999, pp. 1656-1665