Ataxia with oculomotor apraxia type 2 in the Canadian aboriginal population
Clin Genet
.
2016 Apr;89(4):515-516.
doi: 10.1111/cge.12650.
Epub 2015 Aug 31.
Authors
A A Mhanni
1
2
,
J N Hartley
1
,
E Harward
3
,
E Spriggs
1
4
,
F Booth
2
Affiliations
1
Department of Biochemistry and Medical Genetics, University of Manitoba, Manitoba, Canada.
2
Department of Pediatrics and Child Health, University of Manitoba, Manitoba, Canada.
3
Department of Neurology, University of Utah, Salt Lake City, UT, USA.
4
Diagnostic Services Manitoba, Winnipeg, Manitoba, Canada.
PMID:
26332941
DOI:
10.1111/cge.12650
No abstract available
Publication types
Letter