Glycine encephalopathy (nonketotic hyperglycinaemia): Review and update
Author:
Affiliation:
1. ; Department of Pediatrics; University of British Columbia; 4480 Oak St Vancouver, British Columbia V6H 3V4 Canada E-mail
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000031222.38328.59/fullpdf
Reference16 articles.
1. Transient nonketotic hyperglycinemia: two case reports and literature review;Aliefendioglu;Pediatr Neurol,2003
2. Non-concordance of CVS and liver glycine cleavage enzyme in 3 families with NKH leading to false negative prenatal diagnosis;Applegarth;Prenat Diagn,2000
3. Diagnostic clues and outcome of early treatment of NKH;Boneh;Pediatr Neurol,1996
4. Concerns regarding transience and heterozygosity in neonatal hyperglycinemia;Hamosh;Ann Neurol,2003
5. Defective glycine cleavage system in non-ketotic hyperglycinemia;Hiraga;J Clin Invest,1981
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