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Original article
A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima

Authors

  1. 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
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Citation

Koehler K, Milev MP, Prematilake K, et al
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 18, 2017

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