Article info
PDFGenome-wide studies
Original article
A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima
- Correspondence to Dr Katrin Koehler, Division of Paediatric Endocrinology and Diabetology, Department of Paediatrics, Clinical Research, Technical University Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; katrin.koehler{at}uniklinikum-dresden.de
Citation
A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima
Publication history
- Received June 16, 2016
- Revised September 2, 2016
- Accepted September 10, 2016
- First published October 5, 2016.
Online issue publication
February 23, 2017
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