Cargando…
Molecular Approach for Distal Renal Tubular Acidosis Associated AE1 Mutations
The molecular approaches to distal renal tubular acidosis (dRTA) associated AE1 mutations lead us to understand the genetic and pathophysiological aspects of the acidification defects. An unanticipated high value of the urine-blood (U-B) PCO(2) after NaHCO(3) loading observed in a case of dRTA and s...
Autor principal: | Vasuvattakul, Somkiat |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Electrolyte Metabolism
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041492/ https://www.ncbi.nlm.nih.gov/pubmed/21468194 http://dx.doi.org/10.5049/EBP.2010.8.1.25 |
Ejemplares similares
-
Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations
por: Yenchitsomanus, Pa-thai, et al.
Publicado: (2005) -
Red Blood Cell AE1/Band 3 Transports in Dominant Distal Renal Tubular Acidosis Patients
por: Bertocchio, Jean-Philippe, et al.
Publicado: (2020) -
Deafness in distal renal tubular acidosis
Publicado: (2013) -
Familial distal renal tubular acidosis
por: Zhang, Lihong, et al.
Publicado: (2021) -
Distal renal tubular acidosis: a systematic approach from diagnosis to treatment
por: Giglio, Sabrina, et al.
Publicado: (2021)