284 Search for mutations in PO and PMP22 coding sequences...

European Journal of Paediatric Neurology 1999 Vol. 3; Iss. 6

284 Search for mutations in PO and PMP22 coding sequences in CMT1 and sporadic demyelinating CMT without CMT1 a duplication

A. Mantel, V. Planté, M. Tardieu, S. Métral, B. Tabarki, G. Saïd, P. Landrieu
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Volume:
3
Year:
1999
Language:
english
Pages:
1
DOI:
10.1016/s1090-3798(99)91295-3
File:
PDF, 269 KB
english, 1999
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