Monies, D., Vågbø, C. B., Al-Owain, M., Alhomaidi, S., & Alkuraya, F. S. (2019). Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification. Am J Hum Genet.
Citación estilo ChicagoMonies, Dorota, Cathrine Broberg Vågbø, Mohammad Al-Owain, Suzan Alhomaidi, and Fowzan S. Alkuraya. "Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification." Am J Hum Genet 2019.
Cita MLAMonies, Dorota, et al. "Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification." Am J Hum Genet 2019.
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