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

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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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Header DbId: asn
DbLabel: Academic Search Ultimate
An: 154071663
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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  Data: A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency.
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PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=154071663
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.37897/RJP.2021.3.4
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      – Code: eng
        Text: English
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        PageCount: 6
        StartPage: 186
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      – TitleFull: A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency.
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            NameFull: Pintilie, Sebastian Romeo
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            NameFull: Fodor, Adriana
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            NameFull: Bembea, Marius
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            NameFull: Petchesi, Codruța Diana
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            NameFull: Grad, Simona
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            NameFull: Damian, Laura
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            – D: 01
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              Text: 2021
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              Y: 2021
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              Value: 70
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            – TitleFull: Romanian Journal of Pediatrics / Revista Romana de Pediatrie
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