Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Fiona E. Karet(Howard Hughes Medical Institute), Karin E. Finberg(Howard Hughes Medical Institute), Raoul D. Nelson(University of Utah), Ahmet Nayır(Istanbul University), H. Naci Mocan(Karadeniz Technical University), Sami A. Sanjad(King Faisal Specialist Hospital & Research Centre), Juan Rodríguez‐Soriano(Hospital de Cruces), Fernando de Almeida Santos(Universidad de Oviedo), Cor W. R. J. Cremers(Radboud University Nijmegen), Antonio Di Pietro, B I Hoffbrand(Whittington Hospital), Jacek Winiarski(Karolinska Institutet), Ayşı̇n Bakkaloğlu(Hacettepe University), Seza Özen(Hacettepe University), Ruhan Düşünsel(Erciyes University), Paul Goodyer(Montreal Children's Hospital), Sally A. Hulton(Birmingham Children's Hospital), Doris K. Wu(National Institute on Deafness and Other Communication Disorders), Anne B. Skvorak(Brigham and Women's Hospital), Cynthia C. Morton(Brigham and Women's Hospital), Michael J. Cunningham(Massachusetts Eye and Ear Infirmary), Vivekanand Jha(Post Graduate Institute of Medical Education and Research), Richard P. Lifton(Howard Hughes Medical Institute)
Nature Genetics
January 1, 1999
Cited by 691

Abstract


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