Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases
- 1 September 1995
- journal article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 4 (9) , 1673-1674
- https://doi.org/10.1093/hmg/4.9.1673
Abstract
E. LeGuern, R. Gouider, J. Lopes, N. Abbas, M. Gugenheim, S. Tardieu, N. Ravisé, J.-M. Léger, J.-M. Vallat, P. Bouche, Y. Agid, A. Brice, the French CMT CollaboKeywords
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