A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation.
Publication
, Journal Article
Turel, O; Aygun, D; Kardas, M; Torun, E; Hershfield, M; Camcıoglu, Y
Published in: Pediatr Neonatol
February 2018
Duke Scholars
Published In
Pediatr Neonatol
DOI
EISSN
2212-1692
Publication Date
February 2018
Volume
59
Issue
1
Start / End Page
97 / 99
Location
Singapore
Related Subject Headings
- Pediatrics
Citation
APA
Chicago
ICMJE
MLA
NLM
Turel, O., Aygun, D., Kardas, M., Torun, E., Hershfield, M., & Camcıoglu, Y. (2018). A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation. Pediatr Neonatol, 59(1), 97–99. https://doi.org/10.1016/j.pedneo.2016.10.008
Turel, Ozden, Deniz Aygun, Murat Kardas, Emel Torun, Micheal Hershfield, and Yıldız Camcıoglu. “A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation.” Pediatr Neonatol 59, no. 1 (February 2018): 97–99. https://doi.org/10.1016/j.pedneo.2016.10.008.
Turel O, Aygun D, Kardas M, Torun E, Hershfield M, Camcıoglu Y. A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation. Pediatr Neonatol. 2018 Feb;59(1):97–9.
Turel, Ozden, et al. “A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation.” Pediatr Neonatol, vol. 59, no. 1, Feb. 2018, pp. 97–99. Pubmed, doi:10.1016/j.pedneo.2016.10.008.
Turel O, Aygun D, Kardas M, Torun E, Hershfield M, Camcıoglu Y. A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation. Pediatr Neonatol. 2018 Feb;59(1):97–99.
Published In
Pediatr Neonatol
DOI
EISSN
2212-1692
Publication Date
February 2018
Volume
59
Issue
1
Start / End Page
97 / 99
Location
Singapore
Related Subject Headings
- Pediatrics