Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency.
Publication
, Journal Article
Burbank, AJ; Shah, SN; Montgomery, M; Peden, D; Tarrant, TK; Weimer, ET
Published in: Pediatr Allergy Immunol
February 2016
Duke Scholars
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Published In
Pediatr Allergy Immunol
DOI
EISSN
1399-3038
Publication Date
February 2016
Volume
27
Issue
1
Start / End Page
96 / 98
Location
England
Related Subject Headings
- Phenotype
- Pedigree
- Mutation
- Immunologic Deficiency Syndromes
- Humans
- Homozygote
- Guanine Nucleotide Exchange Factors
- Genetic Predisposition to Disease
- Female
- Exome
Citation
APA
Chicago
ICMJE
MLA
NLM
Burbank, A. J., Shah, S. N., Montgomery, M., Peden, D., Tarrant, T. K., & Weimer, E. T. (2016). Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency. Pediatr Allergy Immunol, 27(1), 96–98. https://doi.org/10.1111/pai.12451
Burbank, Allison J., Shaili N. Shah, Maureen Montgomery, David Peden, Teresa K. Tarrant, and Eric T. Weimer. “Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency.” Pediatr Allergy Immunol 27, no. 1 (February 2016): 96–98. https://doi.org/10.1111/pai.12451.
Burbank AJ, Shah SN, Montgomery M, Peden D, Tarrant TK, Weimer ET. Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency. Pediatr Allergy Immunol. 2016 Feb;27(1):96–8.
Burbank, Allison J., et al. “Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency.” Pediatr Allergy Immunol, vol. 27, no. 1, Feb. 2016, pp. 96–98. Pubmed, doi:10.1111/pai.12451.
Burbank AJ, Shah SN, Montgomery M, Peden D, Tarrant TK, Weimer ET. Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency. Pediatr Allergy Immunol. 2016 Feb;27(1):96–98.
Published In
Pediatr Allergy Immunol
DOI
EISSN
1399-3038
Publication Date
February 2016
Volume
27
Issue
1
Start / End Page
96 / 98
Location
England
Related Subject Headings
- Phenotype
- Pedigree
- Mutation
- Immunologic Deficiency Syndromes
- Humans
- Homozygote
- Guanine Nucleotide Exchange Factors
- Genetic Predisposition to Disease
- Female
- Exome