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Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
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Footnotes
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This work was supported by TANDEM grant 3238–056350.99 from the Swiss National Foundation and by grant G.0243.98 from the Foundation for Scientific Research (FWO, Flanders). Collaboration occurred in the context of EUROGLYCAN, a network for CDG research funded by the Fifth Framework Program of the European Commission (QLG1-CT-2000-00047).
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Conflict of interest: none declared.