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pro vyhledávání: '"Bushra Faisal Almugari"'
Autor:
Raghdah Sorour Sorour, Rawan Hassan alsharyoufi, Om hani Malibari, Samia Mahdi Ahmed, Bsma Ali Algarni, Safiah Abdulkarim Alenezi, Alia M. Albalawi, Bushra Faisal Almugari
Publikováno v:
International Journal of Molecular Biology. 3
Background Citrullinemia type is an inherited autosomal recessive disease and a member of Urea Cycle Disorders UCD characterized by accumulation of ammonia in the blood as a result of defect in enzyme called ldquo argininosuccinate synthetase rdquo A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08fd9666bb7cc7c2ad2ab75a88163d53
https://doi.org/10.15406/ijmboa.2018.03.00081
https://doi.org/10.15406/ijmboa.2018.03.00081
