S.C.B. and S.A., M.B. and L.V. contributed equally to this work.
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation
Article first published online: 20 APR 2012
Copyright © 2011 American Neurological Association
Annals of Neurology
Volume 71, Issue 4, pages 509–519, April 2012
How to Cite
Blumen, S. C., Astord, S., Robin, V., Vignaud, L., Toumi, N., Cieslik, A., Achiron, A., Carasso, R. L., Gurevich, M., Braverman, I., Blumen, N., Munich, A., Barkats, M. and Viollet, L. (2012), A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation. Ann Neurol., 71: 509–519. doi: 10.1002/ana.22684
- Issue published online: 20 APR 2012
- Article first published online: 20 APR 2012
- Accepted manuscript online: 27 NOV 2011 11:11PM EST
- Manuscript Accepted: 18 NOV 2011
- Manuscript Revised: 15 OCT 2011
- Manuscript Received: 28 MAY 2010
Additional Supporting Information can be found in the online version of this article.
|ANA_22684_sm_SuppFig1.tif||10131K||Supporting Information Figure 1|
|ANA_22684_sm_SuppTab1.doc||31K||Supplementary table 1: Microatellites markers used for the genotyping of the whole pedigree at the DSMA2 and DSMA1/DSMA3 loci and at the four candidate loci detected by Genscan analysis of patient's DNA.|
|ANA_22684_sm_SuppTab2.doc||42K||Supplementary table 2: Genetic localization and references of the genes sequenced in the study.|
|ANA_22684_sm_SuppTab3.doc||37K||Supplementary table 3: Primer sequences and annealing temperatures for HSJ1 analysis of coding sequences at the genomic and at the transcriptional levels.|
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