Associated Papers
Mutation profiling in eight cases of vagal paragangliomas.
Kudryavtseva AV et al.
Bmc Medical Genomics, 2020
32948195 (PubMed )
Supplement: 12920_2020_763_MOESM1_ESM.xls › Pat4
Functional and structural analysis of rare SLC2A2 variants associated with Fanconi-Bickel syndrome and metabolic traits.
Enogieru OJ et al.
Human Mutation, 2019
Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotype.
Ruggiero JE et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2015
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