Monies D et al. Recessive truncating mutations in ALKBH8 cause intellectual disability and severe impairment of wobble uridine modification. Am J Hum Genet. 2019;104(6):1202–1209. PMID: 31079898.
INTS1
Monies D et al. Recessive truncating mutations in ALKBH8 cause intellectual disability and severe impairment of wobble uridine modification. Am J Hum Genet. 2019;104(6):1202–1209. PMID: 31079898.