VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE

Authors
PAREYSON D MENICHELLA D BOTTI S SGHIRLANZONI A FALLICA E MORA M CIANO C SHY ME TARONI F
Citation
D. Pareyson et al., VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE, Neurology, 50(4), 1998, pp. 8003-8003
Citations number
NO
Categorie Soggetti
Clinical Neurology
Journal title
Neurology → ACNP
ISSN journal
00283878
Volume
50
Issue
4
Year of publication
1998
Supplement
4
Pages
8003 - 8003
Database
ISI
SICI code
0028-3878(1998)50:4<8003:VMCIPH>2.0.ZU;2-V