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pro vyhledávání: '"Saba Fakharianzadeh"'
Autor:
Reza Mola-Ali-Nejad, Saba Fakharianzadeh, Zahra Maloum, Mohammad Taheri, Zeinab Shirvani-Farsani
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 42:527-537
Publikováno v:
Clinical Medicine And Health Research Journal. 2:99-102
Introduction: Argininemia is an autosomal recessive uncommon metabolic condition, caused by mutations in arginase enzyme. Variable clinical symptoms of argininemia might bring about a delayed diagnosis. In order to prove an argininemia condition, a g