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

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Bibliographic Details
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
Description
ISSN:19415923
DOI:10.12659/AJCR.948797