Glycogen storage disease type II risk factors: Difference between revisions
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{{Glycogen storage disease type II}} | {{Glycogen storage disease type II}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{Anmol}} | ||
==Overview== | ==Overview== | ||
The most potent risk factor in the development of glycogen storage disease type 2 is a sibling with glycogen storage disease type 2. | |||
The most potent risk factor in the development of | |||
==Risk Factors== | ==Risk Factors== | ||
The most potent risk factor in the development of glycogen storage disease type 2 is a sibling with glycogen storage disease type 2.<ref>Leslie N, Bailey L. Pompe Disease. 2007 Aug 31 [Updated 2017 May 11]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1261/</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 17:54, 18 January 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Overview
The most potent risk factor in the development of glycogen storage disease type 2 is a sibling with glycogen storage disease type 2.
Risk Factors
The most potent risk factor in the development of glycogen storage disease type 2 is a sibling with glycogen storage disease type 2.[1]
References
- ↑ Leslie N, Bailey L. Pompe Disease. 2007 Aug 31 [Updated 2017 May 11]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1261/