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Article

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

Clinical genetics - 1 Dec 2015

Williams C, Jiang Y-H, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S

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Identifiers

PMID: 25823418
DOI: 10.1111/cge.12581

Genes

PGAP1

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