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Zhou, V. ATP6V0A4 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4822 (accessed on 29 September 2026).
Zhou V. ATP6V0A4 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4822. Accessed September 29, 2026.
Zhou, Vicky. "ATP6V0A4 Gene" Encyclopedia, https://encyclopedia.pub/entry/4822 (accessed September 29, 2026).
Zhou, V. (2020, December 24). ATP6V0A4 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4822
Zhou, Vicky. "ATP6V0A4 Gene." Encyclopedia. Web. 24 December, 2020.
ATP6V0A4 Gene
Edit

ATPase H+ transporting V0 subunit a4

genes

References

  1. Alper SL. Familial renal tubular acidosis. J Nephrol. 2010 Nov-Dec;23 Suppl16:S57-76. Review.
  2. Andreucci E, Bianchi B, Carboni I, Lavoratti G, Mortilla M, Fonda C, BigozziM, Genuardi M, Giglio S, Pela I. Inner ear abnormalities in four patients withdRTA and SNHL: clinical and genetic heterogeneity. Pediatr Nephrol. 2009Nov;24(11):2147-53. doi: 10.1007/s00467-009-1261-3.
  3. Batlle D, Haque SK. Genetic causes and mechanisms of distal renal tubularacidosis. Nephrol Dial Transplant. 2012 Oct;27(10):3691-704. doi:10.1093/ndt/gfs442. Review.
  4. Li X, Chai Y, Tao Z, Li L, Huang Z, Li Y, Wu H, Yang T. Novel mutations inATP6V0A4 are associated with atypical progressive sensorineural hearing loss in aChinese patient with distal renal tubular acidosis. Int J PediatrOtorhinolaryngol. 2012 Jan;76(1):152-4. doi: 10.1016/j.ijporl.2011.10.017.
  5. Stover EH, Borthwick KJ, Bavalia C, Eady N, Fritz DM, Rungroj N, Giersch AB,Morton CC, Axon PR, Akil I, Al-Sabban EA, Baguley DM, Bianca S, Bakkaloglu A,Bircan Z, Chauveau D, Clermont MJ, Guala A, Hulton SA, Kroes H, Li Volti G, MirS, Mocan H, Nayir A, Ozen S, Rodriguez Soriano J, Sanjad SA, Tasic V, Taylor CM, Topaloglu R, Smith AN, Karet FE. Novel ATP6V1B1 and ATP6V0A4 mutations inautosomal recessive distal renal tubular acidosis with new evidence for hearingloss. J Med Genet. 2002 Nov;39(11):796-803.
  6. Vargas-Poussou R, Houillier P, Le Pottier N, Strompf L, Loirat C, Baudouin V, Macher MA, Déchaux M, Ulinski T, Nobili F, Eckart P, Novo R, Cailliez M, Salomon R, Nivet H, Cochat P, Tack I, Fargeot A, Bouissou F, Kesler GR, Lorotte S,Godefroid N, Layet V, Morin G, Jeunemaître X, Blanchard A. Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for earlysensorineural hearing loss associated with mutations in the ATP6V0A4 gene. J AmSoc Nephrol. 2006 May;17(5):1437-43.
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Update Date: 24 Dec 2020
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