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

The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population.

American journal of medical genetics. Part A - 15 Dec 2006

Gutierrez Silvia, Magano Luis, Delicado Alicia, Mori María A, de Torres María L, Fernández Luis, Palomares María, Fernández Eva, Tarduchy Gemma R, Molano Jesús, Gracia Ricardo, Pajares Isidora López, Lapunzina Pablo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Polymorphism, Single Nucleotide
Share to Amino Acid Substitution
Share to Angiogenic Proteins

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

Share to Case-Control Studies

Share to Gene Frequency

Source

Identifiers

PMID: 17103452
DOI: 10.1002/ajmg.a.31532

Genes

AGGF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population.PMID 17103452Read ↗

Polymorphic Variants rs13155212 (T/C) and rs7704267 (G/C) in the AGGF1 Gene and Risk of Varicose Veins of the Lower Extremities in the Population of Ethnic Russians.Semantic proximity Read ↗

AccI polymorphism in von Willebrand factor (F8VWF) at codon 516.Semantic proximity Read ↗

Polymorphism in ficolin-1 (FCN1) gene is associated with an earlier onset of type 1 diabetes mellitus in children and adolescents from northeast Brazil.Semantic proximity Read ↗

Allele frequency distribution of the D1S80 VNTR locus in a Tunisian population.Semantic proximity Read ↗

Allele frequencies for the VNTR locus D17S5 (YNZ22) in Hungary.Semantic proximity Read ↗

Identification of genetic variants in the human thromboxane synthase gene (CYP5A1).Semantic proximity Read ↗

G to A polymorphism in exon 45 of the COL1A1 gene.Semantic proximity Read ↗

Associations of VEGF Gene Polymorphisms With Erectile Dysfunction and Related Risk Factors.Semantic proximity Read ↗

Correlation analysis between ADRB1 gene polymorphism and eclampsia.Semantic proximity Read ↗

Dinucleotide repeat polymorphisms at the D5S257 and D5S268 loci on chromosome 5p.Semantic proximity Read ↗

Allele frequency distribution of 1691G >A F5 (which confers Factor V Leiden) across Europe, including Slavic populations.Semantic proximity Read ↗

Role of VEGF gene variability in longevity: a lesson from the Italian population.Semantic proximity Read ↗

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