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A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.
Piazza, Selina; Baldinotti, Fulvia; Fogli, Antonella; Conidi, Maria Elena; Michelucci, Angela; Ienco, Elena Caldarazzo; Mancuso, Michelangelo; Simi, Paolo; Siciliano, Gabriele.
Affiliation
  • Piazza S; Department of Neuroscience, Neurological Clinic, Pisa, Italy.
Neuromuscul Disord ; 20(12): 817-9, 2010 Dec.
Article in En | MEDLINE | ID: mdl-20850974
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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
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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