Associated Papers
Prevalence of synonymous mutations in m6A modification sites in human cancers.
Chen R et al.
Genes & Diseases, 2025
39524540 (PubMed )
Supplement: mmc3.xlsx › cosmic_GRCH38_DRACH_mutA_overla
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s006.pdf
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