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New disease loci
Original article
Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism

Authors

  1. Correspondence to Professor Aslıhan Tolun, Department of Molecular Biology and Genetics, Boğaziçi University, KP 301, Bebek, Istanbul 34342, Turkey; tolun{at}boun.edu.tr
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Citation

Köroğlu Ç, Seven M, Tolun A
Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism
Journal of Medical Genetics 2013;50:515-520.

Publication history

  • Received March 5, 2013
  • Revised April 15, 2013
  • Accepted April 25, 2013
  • First published June 7, 2013.
Online issue publication 
April 27, 2016

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