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Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report.
Kochanski, A; Drac, H; Jedrzejowska, H; Hausmanowa-Petrusewicz, I.
Affiliation
  • Kochanski A; Neuromuscular Unit, Medical Research Center, Polish Academy of Sciences, Warsaw, Poland. neurmyol@cmdik.pan.pl
Eur J Neurol ; 10(5): 547-9, 2003 Sep.
Article in En | MEDLINE | ID: mdl-12940837
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Collection: 01-internacional Database: MEDLINE Main subject: Asparagine / Charcot-Marie-Tooth Disease / Myelin P0 Protein / Lysine Type of study: Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2003 Document type: Article Affiliation country: Poland Country of publication: United kingdom
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Asparagine / Charcot-Marie-Tooth Disease / Myelin P0 Protein / Lysine Type of study: Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2003 Document type: Article Affiliation country: Poland Country of publication: United kingdom