Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group

Verfasser / Beitragende:
[J. Lopes, E. LeGuern, R. Gouider, S. Tardieu, N. Abbas, N. Birouk, M. Gugenheim, P. Bouche, Y. Agid, A. Brice]
Ort, Verlag, Jahr:
1996
Enthalten in:
American Journal of Human Genetics, 58/6(1996), 1223-1230
Format:
Artikel (online)
ID: 43946160X