Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH)-Reference-Cited by-同舟云学术

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Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH)

Published:2003-08 Issue:4 Volume:79 Page:272-280
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Toone Jennifer R,Applegarth Derek A,Levy Harvey L,Coulter-Mackie Marion B,Lee Gary

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. Nonketotic hyperglycinemia: molecular lesion, diagnosis, and pathophysiology;Tada;J. Inherit Metab. Dis.,1993

2. Biochemical and molecular investigations of patients with nonketotic hyperglycinemia;Toone;Mol. Genet. Metab.,2000

3. Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosis;Applegarth;Mol. Gen. Metab.,2001

4. Nonketotic hyperglycinemia: studies in an atypical variant;Singer;Neurology,1989

5. Nonketotic hyperglycinemia;Hamosh,2001

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