Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.
Journal Article (Letter)
Full Text
Duke Authors
Cited Authors
- Williams, C; Jiang, Y-H; Shashi, V; Crimian, R; Schoch, K; Harper, A; McHale, D; Goldstein, D; Petrovski, S
Published Date
- December 2015
Published In
Volume / Issue
- 88 / 6
Start / End Page
- 597 - 599
PubMed ID
- 25823418
Electronic International Standard Serial Number (EISSN)
- 1399-0004
Digital Object Identifier (DOI)
- 10.1111/cge.12581
Language
- eng
Conference Location
- Denmark