A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.
Neuromuscul Disord
; 20(12): 817-9, 2010 Dec.
Article
in En
| MEDLINE
| ID: mdl-20850974
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myelin P0 Protein
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Female
/
Humans
Language:
En
Journal:
Neuromuscul Disord
Journal subject:
NEUROLOGIA
Year:
2010
Document type:
Article
Affiliation country:
Italia