Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Author： Tazir M.  

Publisher： Oxford University Press

ISSN： 1460-2156

Source： Brain, Vol.127, Iss.1, 2004-01, pp. : 154-163

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Molecular Genetics of Autosomal-Recessive Axonal Charcot-Marie-Tooth Neuropathies

By  

NeuroMolecular Medicine, Vol. 8, Iss. 1-2, 2006-03 ,pp. : 87-106

Humana Press, Inc

Access to resources Recommend Favorite

Autosomal-Recessive Forms of Demyelinating Charcot-Marie-Tooth Disease

By  

NeuroMolecular Medicine, Vol. 8, Iss. 1-2, 2006-03 ,pp. : 75-86

Humana Press, Inc

Access to resources Recommend Favorite

Molecular Genetics of Autosomal-Dominant Axonal Charcot-Marie-Tooth Disease

By  

NeuroMolecular Medicine, Vol. 8, Iss. 1-2, 2006-03 ,pp. : 63-74

Humana Press, Inc

Access to resources Recommend Favorite

Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A

By Krajewski K.M.  

Brain, Vol. 123, Iss. 7, 2000-07 ,pp. : 1516-1527

Oxford University Press

Access to resources Recommend Favorite

Molecular Genetics of Autosomal-Dominant Demyelinating Charcot-Marie-Tooth Disease

By  

NeuroMolecular Medicine, Vol. 8, Iss. 1-2, 2006-03 ,pp. : 43-62

Humana Press, Inc

Access to resources Recommend Favorite