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Novel PGM1 Mutation in Congenital Disorder of Glycosylation Type 1T: A Case Report of Liver Failure and Myopathy.

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Title: Novel PGM1 Mutation in Congenital Disorder of Glycosylation Type 1T: A Case Report of Liver Failure and Myopathy.
Authors: Al-Ahmari, Abdulaziz A.1,2 Aahmari@iau.edu.sa
Source: American Journal of Case Reports. 11/3/2025, Vol. 26, p1-4. 4p.
Database: Academic Search Ultimate
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  Data: Novel PGM1 Mutation in Congenital Disorder of Glycosylation Type 1T: A Case Report of Liver Failure and Myopathy.
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  Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Case+Reports%22">American Journal of Case Reports</searchLink>. 11/3/2025, Vol. 26, p1-4. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=189354654
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        Value: 10.12659/AJCR.948797
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      – Code: eng
        Text: English
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      – TitleFull: Novel PGM1 Mutation in Congenital Disorder of Glycosylation Type 1T: A Case Report of Liver Failure and Myopathy.
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              Text: 11/3/2025
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