Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family

 

Authors
Leal Esquivel, Alejandro; Berghoff, Corinna; Berghoff, Martin; del Valle Carazo, Gerardo; Contreras, Carlos; Montoya, Olga; Hernández, Erick; Barrantes Mesén, Ramiro; Schlötzer Schrehardt, Ursula; Neundörfer, Bernhard; Reis, André; Rautenstrauss, Bernd; Heuss, Dieter
Format
Article
Status
publishedVersion
Description

Publication Year
2003
Language
Topic
Salud pública
Genética
Trastorno neurológico
Fuente
Kérwá
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http://link.springer.com/article/10.1007%2Fs10048-003-0153-0
http://hdl.handle.net/10669/11382
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openAccess
Licencia