Reply
Ann Neurol
.
2017 Feb;81(2):328-329.
doi: 10.1002/ana.24856.
Authors
Katherine L Helbig
1
,
Ulrike B S Hedrich
2
,
Ingrid E Scheffer
3
4
5
,
Ingo Helbig
6
7
,
Holger Lerche
2
,
Johannes R Lemke
8
Affiliations
1
Division of Clinical Genomics, Ambry Genetics, Aliso Viejo, CA.
2
Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
3
Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
4
Florey Institute of Neurosciences and Mental Health, Melbourne, Victoria, Australia.
5
Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia.
6
Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA.
7
Department of Neuropediatrics, University Medical Center Schleswig-Holstein, Department of Neuropediatrics, University of Kiel, Kiel, Germany.
8
Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.
PMID:
28019717
DOI:
10.1002/ana.24856
No abstract available
Publication types
Letter
Comment
MeSH terms
Humans
Mutation
Spastic Paraplegia, Hereditary*