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

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Bibliographic Details
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:	artículo original
Publication Date:	2003
Description:	artículo -- Universidad de Costa Rica. Instituto de Investigaciones en Salud, 2003
Country:	Kérwá
Institution:	Universidad de Costa Rica
Repositorio:	Kérwá
OAI Identifier:	oai:kerwa.ucr.ac.cr:10669/11382
Online Access:	http://link.springer.com/article/10.1007%2Fs10048-003-0153-0 https://hdl.handle.net/10669/11382
Keyword:	Salud pública Genética Trastorno neurológico