Koehler, K. Et Al. 2017. A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima. JOURNAL OF MEDICAL GENETICS , vol.54, no.3 , 176-185.

Koehler, K., Milev, M. P., Prematilake, K., Reschke, F., Kutzner, S., Juehlen, R., ... Landgraf, D.(2017). A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima. JOURNAL OF MEDICAL GENETICS , vol.54, no.3, 176-185.

Koehler, Katrin Et Al. "A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima," JOURNAL OF MEDICAL GENETICS , vol.54, no.3, 176-185, 2017

Koehler, Katrin Et Al. "A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima." JOURNAL OF MEDICAL GENETICS , vol.54, no.3, pp.176-185, 2017

Koehler, K. Et Al. (2017) . "A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima." JOURNAL OF MEDICAL GENETICS , vol.54, no.3, pp.176-185.

@article{article, author={Katrin Koehler Et Al. }, title={A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima}, journal={JOURNAL OF MEDICAL GENETICS}, year=2017, pages={176-185} }