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- Title
Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.
- Authors
Williams, C.; Jiang, Y.‐H.; Shashi, V.; Crimian, R.; Schoch, K.; Harper, A.; McHale, D.; Goldstein, D.; Petrovski, S.
- Abstract
A letter to the editor is presented in response to the article "Null mutation in PGAP1 impairing Gpi-anchor maturation in patients with intellectual disability and encephalopathy," by Y. Murakami and colleagues in the 2014 issue.
- Subjects
GLYCOSYLPHOSPHATIDYLINOSITOL; INTELLECTUAL disabilities; MURAKAMI, Y.
- Publication
Clinical Genetics, 2015, Vol 88, Issue 6, p597
- ISSN
0009-9163
- Publication type
Article
- DOI
10.1111/cge.12581