Associated Papers
Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.
Li Y et al.
Molecular Medicine Reports, 2020
32705272 (PubMed )
Supplement: Supplementary_Data1.xlsx › original
Analysis of variants and mutations in the human winged helix FOXA3 gene and associations with metabolic traits.
Adler-Wailes DC et al.
International Journal of Obesity (2005), 2015
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