Rohrer, J. D., Beck, J., Plagnol, V., Gordon, E., Lashley, T., Revesz, T., . . . Schott, J. M. (2013). Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia. BMJ Publishing Group.
Chicago ZitierstilRohrer, Jonathan D., et al. Exome Sequencing Reveals a Novel Partial Deletion in the Progranulin Gene Causing Primary Progressive Aphasia. BMJ Publishing Group, 2013.
MLA ZitierstilRohrer, Jonathan D., et al. Exome Sequencing Reveals a Novel Partial Deletion in the Progranulin Gene Causing Primary Progressive Aphasia. BMJ Publishing Group, 2013.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.