Case report: A case of SLC26A4 mutations causing pendred syndrome and non-cystic fibrosis bronchiectasis

Overview of attention for article published in Frontiers in Pediatrics, January 2023

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Case report: A case of SLC26A4 mutations causing pendred syndrome and non-cystic fibrosis bronchiectasis https://t.co/dc2nwppxhx

15 Feb 2023

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New Research: Case report: A case of SLC26A4 mutations causing pendred syndrome and non-cystic fibrosis bronchiectasis: The SLC26A4 gene encodes the transmembrane protein pendrin, which is involved in the ion transport of chloride (Cl-),… https://t.co/dHqp

15 Feb 2023

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