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Article

Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile.

Reproductive sciences (Thousand Oaks, Calif.) - 1 Oct 2013

Suazo José, Pardo Rosa, Castillo Silvia, Martin Luz Maria, Rojas Francisca, Santos José Luis, Rotter Karin, Solar Margarita, Tapia Eva

Abstract excerpt

Obese/diabetic mothers present a higher risk to develop offspring with myelomeningocele (MM), evidence supporting the role of energy homeostasis-related genes in neural tube defects. Using polymerase chain reaction-restriction fragment length polymorphism, we have genotyped SLC2A1, HK1, and LEPR single-nucleotide polymorphisms in 105 Chilean patients with MM and their parents in order to evaluate allele-phenotype...

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Source

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Identifiers

PMID: 23427181
DOI: 10.1177/1933719113477489
PMCID: PMC3766345

Genes

LEPR

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.

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