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pro vyhledávání: '"Karin Leckström"'
Autor:
Julia Lindgren, Niklas Darin, Karin Leckström, Gabriella Almén, Jorge Asin-Cayuela, Per Sikora
Publikováno v:
European journal of human genetics : EJHG. 26(6)
γ-Glutamyl transpeptidase deficiency (glutathionuria, OMIM 231950) is a rare disease, with only six patients reported in the literature, although this condition has probably been underdiagnosed due the difficulty to routinely analyze glutathione in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c41d6d7d71396b64740573ef255cdc4
https://pubmed.ncbi.nlm.nih.gov/29483667
https://pubmed.ncbi.nlm.nih.gov/29483667
