Associated Papers
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.
Tian WT et al.
Neuromuscular Disorders : Nmd, 2019
Limitations of galactose therapy in phosphoglucomutase 1 deficiency.
Nolting K et al.
Molecular Genetics and Metabolism Reports, 2017
Select a paper to view details