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Homozygous and compound heterozygous mutations in the ATP6V1B1 gene in patients with renal tubular acidosis and sensorineural hearing loss.
Mohebbi, N; Vargas-Poussou, R; Hegemann, S C A; Schuknecht, B; Kistler, A D; Wüthrich, R P; Wagner, C A.
Affiliation
  • Mohebbi N; Institute of Physiology and Zurich Center for Integrative Human Physiology (ZIHP), University of Zurich, Zurich, Switzerland. nmohebbi@access.uzh.ch
Clin Genet ; 83(3): 274-8, 2013 Mar.
Article in En | MEDLINE | ID: mdl-22509993
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acidosis, Renal Tubular / Vacuolar Proton-Translocating ATPases / Hearing Loss, Sensorineural / Mutation Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Clin Genet Year: 2013 Document type: Article Affiliation country: Suiza Country of publication: Dinamarca
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Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acidosis, Renal Tubular / Vacuolar Proton-Translocating ATPases / Hearing Loss, Sensorineural / Mutation Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Clin Genet Year: 2013 Document type: Article Affiliation country: Suiza Country of publication: Dinamarca