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pro vyhledávání: '"Mohammed Chemsi"'
Autor:
Mohammed Chemsi, Asmaa Biaz, Samira El Machtani-Idrissi, Sophia Tazi, Sanae Bouhsain, Abdellah Dami
Publikováno v:
Clinical Laboratory. 66
Hereditary xanthinuria was the first inherited purine metabolism disorder described. It is a rare pathology, which is most often asymptomatic and whose incidence is therefore underestimated. We report the case of a patient with an undetectable level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9667e1b9360b2e6d849447be2ce207f8
https://doi.org/10.7754/clin.lab.2020.200253
https://doi.org/10.7754/clin.lab.2020.200253
