Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.

Published

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

Pubmed Central ID

  • 25823418

Electronic International Standard Serial Number (EISSN)

  • 1399-0004

Digital Object Identifier (DOI)

  • 10.1111/cge.12581

Language

  • eng

Conference Location

  • Denmark