Associated Papers
A missense variant in FTCD is associated with arsenic metabolism and toxicity phenotypes in Bangladesh.
Pierce BL et al.
Plos Genetics, 2019
Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.
Skarp S et al.
Plos One, 2018
30157244 (PubMed )
Supplement: pone.0203313.s001.xlsx › Family8_SNPs
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