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Springer (part of Springer Nature), neurogenetics, 4(4), p. 191-197
DOI: 10.1007/s10048-003-0153-0
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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
Journal article published in 2003 by
Alejandro Leal,
Corinna Berghoff,
Martin Berghoff,
Gerardo Del Valle,
Carlos Contreras,
Olga Montoya,
Erick Hern�ndez,
Ramiro Barrantes,
Ursula Schl�tzer-Schrehardt,
Bernhard Neund�rfer,
Andr� Reis 
,
Bernd Rautenstrauss,
Dieter Heuss
,
Bernd Rautenstrauss,
Dieter Heuss
This paper is available in a repository.
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