3 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 32053088 | Sialuria-Related Intellectual Disability in Children and Adolescent of Pakistan: Tenth Patient Described has a Novel Mutation in the GNE Gene. | 2020 | 1 |
| 2 | 15987957 | Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. | 2005 Nov | 2 |
| 3 | 12450772 | Magnesium may help patients with recessive hereditary inclusion body myopathy, a pathological review. | 2003 Jan | 1 |