Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency.
Publication
, Journal Article
Bollinger, ME; Arredondo-Vega, FX; Santisteban, I; Schwarz, K; Hershfield, MS; Lederman, HM
Published in: N Engl J Med
May 23, 1996
Duke Scholars
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Published In
N Engl J Med
DOI
ISSN
0028-4793
Publication Date
May 23, 1996
Volume
334
Issue
21
Start / End Page
1367 / 1371
Location
United States
Related Subject Headings
- Severe Combined Immunodeficiency
- Mutation
- Molecular Sequence Data
- Male
- Jaundice, Neonatal
- Infant, Newborn
- Humans
- Hepatitis
- General & Internal Medicine
- DNA, Complementary
Citation
APA
Chicago
ICMJE
MLA
NLM
Bollinger, M. E., Arredondo-Vega, F. X., Santisteban, I., Schwarz, K., Hershfield, M. S., & Lederman, H. M. (1996). Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency. N Engl J Med, 334(21), 1367–1371. https://doi.org/10.1056/NEJM199605233342104
Bollinger, M. E., F. X. Arredondo-Vega, I. Santisteban, K. Schwarz, M. S. Hershfield, and H. M. Lederman. “Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency.” N Engl J Med 334, no. 21 (May 23, 1996): 1367–71. https://doi.org/10.1056/NEJM199605233342104.
Bollinger ME, Arredondo-Vega FX, Santisteban I, Schwarz K, Hershfield MS, Lederman HM. Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency. N Engl J Med. 1996 May 23;334(21):1367–71.
Bollinger, M. E., et al. “Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency.” N Engl J Med, vol. 334, no. 21, May 1996, pp. 1367–71. Pubmed, doi:10.1056/NEJM199605233342104.
Bollinger ME, Arredondo-Vega FX, Santisteban I, Schwarz K, Hershfield MS, Lederman HM. Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency. N Engl J Med. 1996 May 23;334(21):1367–1371.
Published In
N Engl J Med
DOI
ISSN
0028-4793
Publication Date
May 23, 1996
Volume
334
Issue
21
Start / End Page
1367 / 1371
Location
United States
Related Subject Headings
- Severe Combined Immunodeficiency
- Mutation
- Molecular Sequence Data
- Male
- Jaundice, Neonatal
- Infant, Newborn
- Humans
- Hepatitis
- General & Internal Medicine
- DNA, Complementary