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Brain. 2014 Jul;137(Pt 7):e286. doi: 10.1093/brain/awu091. Epub 2014 Apr 15.

A novel missense mutation confirms ATL3 as a gene for hereditary sensory neuropathy type 1.

Author information

  • 11 Department of Neurology, University of Basel Hospital, 4031 Basel, Switzerland2 Division of Neuropaediatrics, University of Basel Childrens Hospital, 4056 Basel, Switzerland.
  • 23 Department of Orthopaedics, Medical University Vienna, 1090 Vienna, Austria.
  • 34 Institute of Human Genetics, Helmholtz Zentrum München - German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • 44 Institute of Human Genetics, Helmholtz Zentrum München - German Research Center for Environmental Health, 85764 Neuherberg, Germany5 Institute for Human Genetics, Technical University Munich, 81675 Munich, Germany.
  • 53 Department of Orthopaedics, Medical University Vienna, 1090 Vienna, Austria michaela.auer-grumbach@meduniwien.ac.at.
PMID:
24736309
[PubMed - indexed for MEDLINE]
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