Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.
Publication
, Journal Article
Williams, C; Jiang, Y-H; Shashi, V; Crimian, R; Schoch, K; Harper, A; McHale, D; Goldstein, D; Petrovski, S
Published in: Clin Genet
December 2015
Duke Scholars
Published In
Clin Genet
DOI
EISSN
1399-0004
Publication Date
December 2015
Volume
88
Issue
6
Start / End Page
597 / 599
Location
Denmark
Related Subject Headings
- Sequence Analysis, DNA
- Phosphoric Monoester Hydrolases
- Membrane Proteins
- Male
- Magnetic Resonance Imaging
- Language Development Disorders
- Humans
- Genotype
- Genetics & Heredity
- Genetic Predisposition to Disease
Citation
APA
Chicago
ICMJE
MLA
NLM
Williams, C., Jiang, Y.-H., Shashi, V., Crimian, R., Schoch, K., Harper, A., … Petrovski, S. (2015). Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy. Clin Genet, 88(6), 597–599. https://doi.org/10.1111/cge.12581
Williams, C., Y. -. H. Jiang, V. Shashi, R. Crimian, K. Schoch, A. Harper, D. McHale, D. Goldstein, and S. Petrovski. “Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.” Clin Genet 88, no. 6 (December 2015): 597–99. https://doi.org/10.1111/cge.12581.
Williams C, Jiang Y-H, Shashi V, Crimian R, Schoch K, Harper A, et al. Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy. Clin Genet. 2015 Dec;88(6):597–9.
Williams, C., et al. “Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.” Clin Genet, vol. 88, no. 6, Dec. 2015, pp. 597–99. Pubmed, doi:10.1111/cge.12581.
Williams C, Jiang Y-H, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S. Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy. Clin Genet. 2015 Dec;88(6):597–599.
Published In
Clin Genet
DOI
EISSN
1399-0004
Publication Date
December 2015
Volume
88
Issue
6
Start / End Page
597 / 599
Location
Denmark
Related Subject Headings
- Sequence Analysis, DNA
- Phosphoric Monoester Hydrolases
- Membrane Proteins
- Male
- Magnetic Resonance Imaging
- Language Development Disorders
- Humans
- Genotype
- Genetics & Heredity
- Genetic Predisposition to Disease