Bhoj, E., Li, D., Harr, M., Edvardson, S., Elpeleg, O., Chisholm, E., . . . Hakonarson, H. (2016). Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia. Am J Hum Genet.
Chicago ZitierstilBhoj, Elizabeth J., et al. "Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia." Am J Hum Genet 2016.
MLA ZitierstilBhoj, Elizabeth J., et al. "Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia." Am J Hum Genet 2016.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.