Glycine

solute carrier family 26 member 3 ; Homo sapiens







2 Article(s)
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1 33599438 Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis. 2021 1
2 33191723 Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis. 2020 Nov 16 1