Zobrazeno 1 - 3
of 3
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
Autor:
Mola-Ali-Nejad, Reza1 (AUTHOR), Fakharianzadeh, Saba2 (AUTHOR), Maloum, Zahra2 (AUTHOR), Taheri, Mohammad3 (AUTHOR), Shirvani-Farsani, Zeinab2 (AUTHOR)
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 2023, Vol. 42 Issue 7, p527-537. 11p.