Williams_2015_Clin.Genet_88_597

Reference

Title : Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy -
Author(s) : Williams C , Jiang YH , Shashi V , Crimian R , Schoch K , Harper A , McHale D , Goldstein D , Petrovski S
Ref : Clin Genet , 88 :597 , 2015
PubMedID: 25823418

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Citations formats

Williams C, Jiang YH, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S (2015)
Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy
Clin Genet 88 :597

Williams C, Jiang YH, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S (2015)
Clin Genet 88 :597