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Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
- Correspondence to: G Matthijs Center for Human Genetics, University of Leuven, Herestraat 49, B-3000 Leuven, Belgium; Gert.Matthijsuz.kuleuven.ac.be
Citation
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
Publication history
- Received December 4, 2003
- Accepted February 6, 2004
- First published July 2, 2004.
Online issue publication
July 02, 2004
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Copyright 2004 Journal of Medical Genetics