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Verification of diagnosis in a 17-year-old boy with clinical glycogen storage disease type Ia by mutation screening |
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| Authors: | D. Matern H. Niederhoff M. Brandis J. Y. Chou |
| Affiliation: | (1) Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA;(2) University Children's Hospital, Mathildenstr. 1, 79106 Freiburg, Germany |
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