Wedatilake, Y., Niazi, R., Fassone, E., Powell, C. A., Pearce, S., Plagnol, V., . . . Rahman, S. (2016). TRNT1 deficiency: Clinical, biochemical and molecular genetic features. Orphanet J Rare Dis.
Dyfyniad Arddull ChicagoWedatilake, Yehani, et al. "TRNT1 Deficiency: Clinical, Biochemical and Molecular Genetic Features." Orphanet J Rare Dis 2016.
Dyfyniad MLAWedatilake, Yehani, et al. "TRNT1 Deficiency: Clinical, Biochemical and Molecular Genetic Features." Orphanet J Rare Dis 2016.
Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.