Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis.
Publication
, Journal Article
Johnson, AO; Goldstein, JL; Bali, D
Published in: J Pediatr Gastroenterol Nutr
July 2012
Duke Scholars
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Published In
J Pediatr Gastroenterol Nutr
DOI
EISSN
1536-4801
Publication Date
July 2012
Volume
55
Issue
1
Start / End Page
90 / 92
Location
United States
Related Subject Headings
- Phosphorylase Kinase
- Mutation, Missense
- Male
- Liver Cirrhosis
- Infant
- Humans
- Glycogen Storage Disease
- Gastroenterology & Hepatology
- 3213 Paediatrics
- 3210 Nutrition and dietetics
Citation
APA
Chicago
ICMJE
MLA
NLM
Johnson, A. O., Goldstein, J. L., & Bali, D. (2012). Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis. J Pediatr Gastroenterol Nutr, 55(1), 90–92. https://doi.org/10.1097/MPG.0b013e31823276ea
Johnson, Abiodun O., Jennifer L. Goldstein, and Deeksha Bali. “Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis.” J Pediatr Gastroenterol Nutr 55, no. 1 (July 2012): 90–92. https://doi.org/10.1097/MPG.0b013e31823276ea.
Johnson AO, Goldstein JL, Bali D. Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis. J Pediatr Gastroenterol Nutr. 2012 Jul;55(1):90–2.
Johnson, Abiodun O., et al. “Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis.” J Pediatr Gastroenterol Nutr, vol. 55, no. 1, July 2012, pp. 90–92. Pubmed, doi:10.1097/MPG.0b013e31823276ea.
Johnson AO, Goldstein JL, Bali D. Glycogen storage disease type IX: novel PHKA2 missense mutation and cirrhosis. J Pediatr Gastroenterol Nutr. 2012 Jul;55(1):90–92.
Published In
J Pediatr Gastroenterol Nutr
DOI
EISSN
1536-4801
Publication Date
July 2012
Volume
55
Issue
1
Start / End Page
90 / 92
Location
United States
Related Subject Headings
- Phosphorylase Kinase
- Mutation, Missense
- Male
- Liver Cirrhosis
- Infant
- Humans
- Glycogen Storage Disease
- Gastroenterology & Hepatology
- 3213 Paediatrics
- 3210 Nutrition and dietetics