γ-COPI mediates the retention of kAE1 G701D protein in Golgi apparatus – A mechanistic explanation of distal renal tubular acidosis associated with the G701D mutation
© 2017 The Author(s); published by Portland Press Limited on behalf of the Biochemical Society. Mutations of the solute carrier family 4 member 1 (SLC4A1) gene encoding kidney anion (chloride/bicarbonate ion) exchanger 1 (kAE1) can cause genetic distal renal tubular acidosis (dRTA). Different SLC4A1...
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Main Authors: | , , , , , , , , |
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Format: | Article |
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2018
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Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/41833 |
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Institution: | Mahidol University |
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