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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Bibliografski detalji
Autori:	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
Datum izdanja:	2003
Opis:	artículo -- Universidad de Costa Rica. Instituto de Investigaciones en Salud, 2003
Zemlja:	Kérwá
Institucija:	Universidad de Costa Rica
Repositorio:	Kérwá
OAI Identifier:	oai:kerwa.ucr.ac.cr:10669/11382
Online pristup:	http://link.springer.com/article/10.1007%2Fs10048-003-0153-0 https://hdl.handle.net/10669/11382
Access Level:	acceso abierto
Ključna riječ:	Salud pública Genética Trastorno neurológico