Novel Mutation of Gene Observed in Congenital Chloride Diarrhea
Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene on chromosome 7q31. Affected neonates are vulnerable to dehydration, electrolyte imbalance in the form of hyponatremia, metabolic alkalosis, failure to...
Main Authors: | Ji Hye Cheon, Na Li Yu, Na Mi Lee |
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Format: | Article |
Language: | English |
Published: |
Korean Society of Neonatology
2023-08-01
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Series: | Neonatal Medicine |
Subjects: | |
Online Access: | http://neo-med.org/upload/pdf/nm-2023-30-3-75.pdf |
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