Reasons Charcot–Marie–Tooth disease due to mutations in the MME gene should not be named AR‐CMT2T

E-ISSN： 1531-8249|80|3|477-477

ISSN： 0364-5134

Source： ANNALS OF NEUROLOGY, Vol.80, Iss.3, 2016-09, pp. : 477-477

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

Related content

The EGR2 gene is involved in axonal Charcot−Marie−Tooth disease

EUROPEAN JOURNAL OF NEUROLOGY, Vol. 22, Iss. 12, 2015-12 ,pp. : 1548-1555

John Wiley & Sons Inc

Access to resources Recommend Favorite

Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease

By Fledrich Robert Stassart Ruth M. Sereda Michael W.

British Medical Bulletin, Vol. 102, Iss. 1, 2012-06 ,pp. : 89-113

Oxford University Press

Access to resources Recommend Favorite

Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, Vol. 19, Iss. 3, 2014-09 ,pp. : 242-245

John Wiley & Sons Inc

Access to resources Recommend Favorite

Rigid spine syndrome associated with sensory‐motor axonal neuropathy resembling Charcot–Marie‐Tooth disease is characteristic of Bcl‐2‐associated athanogene‐3 gene mutations even without cardiac involvement

MUSCLE AND NERVE, Vol. 57, Iss. 2, 2018-02 ,pp. : 330-334

John Wiley & Sons Inc

Access to resources Recommend Favorite

Intraneural GJB1 gene delivery improves nerve pathology in a model of X‐linked Charcot–Marie–Tooth disease

ANNALS OF NEUROLOGY, Vol. 78, Iss. 2, 2015-08 ,pp. : 303-316

John Wiley & Sons Inc

Access to resources Recommend Favorite