Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy.
Carbonic anhydrase II (CAII) deficiency in humans is associated with a syndrome of renal tubular acidosis, osteopetrosis, and cerebral calcification. A strain of mice of CAII deficiency due to a point mutation also manifests renal tubular acidosis. We report here that retrograde injection of cationi...
שמור ב:
| הוצא לאור ב: | J Clin Invest |
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| Principais autores: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
1998
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508709/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9525974/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI1694 |
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