Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders? - Wikidata - wikimedia - TriplyDB

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

http://www.wikidata.org/entity/Q33554806

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Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.Differential expression of NPM, GSTA3, and GNMT in mouse liver following long-term irradiation by means of uranium tailings

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Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

http://www.wikidata.org/entity/Q33554806

description

2016 nî lūn-bûn

@nan

2016 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@ast

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@en

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@nl

type

label

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@ast

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@en

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@nl

prefLabel

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@ast

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@en

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@nl

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P1433

Journal of Inherited Metabolic Disorders Reports

P1476

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

@en

P2093

Halil Saglam

http://www.w3.org/2001/XMLSchema#string

Ivo Barić

http://www.w3.org/2001/XMLSchema#string

Ksenija Fumić

http://www.w3.org/2001/XMLSchema#string

Mila Lovrić

http://www.w3.org/2001/XMLSchema#string

Oliver Vugrek

http://www.w3.org/2001/XMLSchema#string

Robert Belužić

http://www.w3.org/2001/XMLSchema#string

Sahin Erdol

http://www.w3.org/2001/XMLSchema#string

P2860

Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.

Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency.

Glycine N-methyltransferase-/- mice develop chronic hepatitis and glycogen storage disease in the liver

Characterization of glycine-N-methyltransferase-gene expression in human hepatocellular carcinoma.

Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.

Glycine N -methyltransferase deficiency: a new patient with a novel mutation.

S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism

Cerebral edema associated with betaine treatment in classical homocystinuria.

Glycine N-methyltransferase and regulation of S-adenosylmethionine levels.

Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function

P304

101-106

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P31

scholarly article

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10.1007/8904_2016_543

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P478

31

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P577

2016-05-21T00:00:00Z

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27207470

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P921

glycine N-methyltransferase deficiency

P932

5388635

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