
A Common Variant in MTHFD1L is Associated with Increased Risk for Spina Bifida
Publication year - 2018
Publication title -
journal of molecular and clinical medicine
Language(s) - English
Resource type - Journals
eISSN - 2617-5282
pISSN - 2616-3632
DOI - 10.31083/j.jmcm.2018.01.003
Subject(s) - spina bifida , neural tube , allele , neural tube defect , medicine , genetics , multifactorial inheritance , population , pediatrics , biology , gene , genotype , single nucleotide polymorphism , environmental health , embryo