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

Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata.

Neuroscience letters - 10 Apr 2009

Dutta Samikshan, Chatterjee Arpita, Sinha Swagata, Chattopadhyay Anindita, Mukhopadhyay Kanchan

Abstract excerpt

Deficiency in cystathionine beta synthase (CBS) enzyme sometimes leads to hyperhomocysteinemia/homocystinuria, conditions often associated with mental retardation (MR). In this investigation, association of idiopathic MR (IMR) with six CBS gene polymorphisms and fasting total plasma homocysteine (plHcy) was explored. Nuclear families with IMR probands (N=180) and control subjects (N=106) were recruited. Genomic...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Cystathionine beta-Synthase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Homocysteine

Share to Intellectual Disability

Share to Sex Factors

Share to White People

Share to Young Adult

Source

Identifiers

PMID: 19429038
DOI: 10.1016/j.neulet.2009.02.040

Genes

CBS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata.PMID 19429038Read ↗

Screening for methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Indian patients with idiopathic mental retardation.Semantic proximity Read ↗

Cystathionine β-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded childrenSemantic proximity Read ↗

Association of MTHFR and RFC1 gene polymorphism with hyperhomocysteinemia and its modulation by vitamin B12 and folic acid in an Indian population.Semantic proximity Read ↗

Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands.Semantic proximity Read ↗

Polymorphisms in MTHFR, MS and CBS genes and homocysteine levels in a Pakistani population.Semantic proximity Read ↗

MTHFR gene polymorphism and its relationship with plasma homocysteine and folate in a North Indian population.Semantic proximity Read ↗

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.Semantic proximity Read ↗

Genetic defects as important factors for moderate hyperhomocysteinemia.Semantic proximity Read ↗

Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate.Semantic proximity Read ↗

Lower incidence of nonsyndromic cleft lip with or without cleft palate in females: is homocysteine a factor?Semantic proximity Read ↗

The frequency of Raynaud’s phenomenon in patients with methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemiaSemantic proximity Read ↗

CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children.Semantic proximity Read ↗

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