Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

door Stover, E, Borthwick, K, Bavalia, C, Eady, N, Fritz, D, Rungroj, N, Giersch, A, Morton, C, Axon, P, Akil, I, Al-Sabban, E, Baguley, D, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M, Guala, A, Hulton, S, Kroes, H, Li, V, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez, S, Sanjad, S, Tasic, V, Taylor, C, Topaloglu, R, Smith, A, Karet, F
Gepubliceerd in 2002