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Objective: The purpose of this study is to explore the relationship between parents' phubbing behavior and children's online gaming time. More importantly, we investigated the mediating role of electronic health literacy in this association.

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Coagulation abnormalities and vascular complications are common in PGM1-CDG.

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Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA; Department of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Department of Biophysics, University of Pécs Medical School, 7624 Pécs, Hungary. Electronic address:

Phosphoglucomutase-1-congenital disorder of glycosylation (PGM1-CDG) is a rare genetic disorder caused by biallelic variants in the PGM1 gene, leading to the deficiency of the PGM1 enzyme. The most common clinical presentations include muscle involvement, failure to thrive, cleft palate, and cardiac involvement. Abnormal serum N-glycosylation, hypoglycemia, and liver function abnormalities including coagulation abnormalities are the most common laboratory abnormalities.

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National, regional, and global estimates of low birthweight in 2020, with trends from 2000: a systematic analysis.

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Division of Data, Analytics, Planning and Monitoring, United Nations Children's Fund, New York, NY, USA.

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