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

Journal Article (Letter)

Full Text

Duke Authors

Shashi, Vandana

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

Clin Genet

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