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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Autori: | , , , , , , , , , , , , |
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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 |
Ključna riječ: | Salud pública Genética Trastorno neurológico |