Associated Papers
Whole exon screening of SLC2A4 gene and the association of rs5435 with type 2 diabetes in a Bangladeshi case-control study.
Rashid MM et al.
Journal, Genetic Engineering & Biotechnology, 2025
Reprogramming Captures the Genetic and Tumorigenic Properties of Neurofibromatosis Type 1 Plexiform Neurofibromas.
Carrió M et al.
Stem Cell Reports, 2019
30713041 (PubMed )
Supplement: mmc2.xls › ALL_SAMPLES.filtered.variants.t
Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation.
Wang Y et al.
Human Mutation, 2000
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