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A 10 bp Deletion Polymorphism and 2 New Variations in the GLUT1 Gene Associated With Meningomyelocele

We sought to examine the diversity and extent of sequence variations in GLUT1 in patients with myelomeningocele (MM) and to identify variations conferring risk of MM. Sequences of the 10 exons and exon-intron boundaries of GLUT1 for 96 patients with MM (48 Caucasians and 48 Mexican Americans) were d...

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Hlavní autoři: Cormier, Clint M., Au, Kit Sing, Northrup, Hope
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3117222/
https://ncbi.nlm.nih.gov/pubmed/21135204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1933719110388293
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