Glial mitochondropathy in infantile neuroaxonal dystrophy: pathophysiological and therapeutic implications
Brain
.
2016 Dec;139(Pt 12):e67.
doi: 10.1093/brain/aww174.
Epub 2016 Aug 6.
Authors
Michelle A Farrar
1
2
,
Hooi Ling Teoh
3
2
,
Susan Brammah
4
,
Tony Roscioli
5
6
7
,
Michael Cardamone
3
2
Affiliations
1
1 Department of Neurology, Sydney Children's Hospital, Sydney, Australia m.farrar@unsw.edu.au.
2
2 Discipline of Paediatrics, School of Women's and Children's Health, UNSW Medicine, The University of New South Wales, Sydney, Australia.
3
1 Department of Neurology, Sydney Children's Hospital, Sydney, Australia.
4
3 Electron Microscope Unit, Anatomical Pathology, Concord Hospital, Concord, Australia.
5
4 Kinghorn Centre for Clinical Genomics, Darlinghurst, NSW, Australia; GOLD Service, Royal North Shore Hospital, Sydney, Australia.
6
5 South Eastern Area Laboratory Services Haematology and Genetics Laboratory, Prince of Wales Hospital, Sydney, Australia.
7
6 Department of Medical Genetics, Sydney Children's Hospital, Sydney Australia.
PMID:
27497490
DOI:
10.1093/brain/aww174
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Axons
Humans
Neuroaxonal Dystrophies*
Neuroglia*