Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Inherited disorders in the conversion of methionine to homocysteine

7 Jul 2009

Abstract excerpt

During the last decade much important new information relating to the metabolic pathway from methionine to homocysteine has been gained. Interest has been stimulated by the discovery of two novel disorders, glycine N-methyltransferase deficiency and S-adenosylhomocysteine hydrolase deficiency. Another disorder in this pathway, methionine adenosyltransferase deficiency, has been increasingly detected, thanks to...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biochemical and Molecular Research
Share to Folate and B Vitamins Research
Share to Metabolism and Genetic Disorders

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19585268
DOI: 10.1007/s10545-009-1146-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited disorders in the conversion of methionine to homocysteinePMID 19585268Read ↗

Genetics of homocysteine metabolism and associated disordersSemantic proximity Read ↗

Genetics of homocysteine metabolism and associated disordersSemantic proximity Read ↗

Hypermethioninemias of genetic and non‐genetic origin: A reviewSemantic proximity Read ↗

Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defectsSemantic proximity Read ↗

Genetic defects in folate and cobalamin pathways affecting the brain.Semantic proximity Read ↗

Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolismSemantic proximity Read ↗

Dysregulation of Epigenetic Mechanisms of Gene Expression in the Pathologies of HyperhomocysteinemiaSemantic proximity Read ↗

Analysis of five cases of hypermethioninemia diagnosed by neonatal screening.Semantic proximity Read ↗

Human biochemical genetics: an insight into inborn errors of metabolism.Semantic proximity Read ↗

Molecular genetics of homocysteine metabolism.Semantic proximity Read ↗

The Spectrum of Mutations of Homocystinuria in the MENA Region.Semantic proximity Read ↗

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based ApproachSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.