A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency.

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Bibliographic Details
Title: A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency.
Authors: Pintilie, Sebastian Romeo1, Fodor, Adriana2,3, Bembea, Marius4,5, Petchesi, Codruța Diana4, Grad, Simona6,7, Damian, Laura8,9, Vulturar, Romana10,11 romanavulturar@gmail.com
Source: Romanian Journal of Pediatrics / Revista Romana de Pediatrie. 2021, Vol. 70 Issue 3, p186-191. 6p.
Database: Academic Search Ultimate
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