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Contribution of copy number variations in CMT1X: a retrospective study.
Capponi, S; Geroldi, A; Pezzini, I; Gulli, R; Ciotti, P; Ursino, G; Lamp, M; Reni, L; Schenone, A; Grandis, M; Mandich, P; Bellone, E.
Affiliation
  • Capponi S; Section of Medical Genetics, Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Eur J Neurol ; 22(2): 406-9, 2015 Feb.
Article in En | MEDLINE | ID: mdl-24724718
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Gene Deletion / Connexins / DNA Copy Number Variations Type of study: Observational_studies / Prognostic_studies Limits: Female / Humans / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2015 Document type: Article Affiliation country: Italy Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Gene Deletion / Connexins / DNA Copy Number Variations Type of study: Observational_studies / Prognostic_studies Limits: Female / Humans / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2015 Document type: Article Affiliation country: Italy Country of publication: United kingdom