Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1‐related nemaline myopathy (NEM3)

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8249|83|2|269-282

ISSN： 0364-5134

Source： ANNALS OF NEUROLOGY, Vol.83, Iss.2, 2018-02, pp. : 269-282

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

Sporadic late‐onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset

By  

MUSCLE AND NERVE, Vol. 51, Iss. 5, 2015-05 ,pp. : 772-774

John Wiley & Sons Inc

Access to resources Recommend Favorite

Whole‐body muscle magnetic resonance imaging in SEPN1‐related myopathy shows a homogeneous and recognizable pattern

By  

MUSCLE AND NERVE, Vol. 52, Iss. 5, 2015-11 ,pp. : 728-735

John Wiley & Sons Inc

Access to resources Recommend Favorite

Whole‐body muscle magnetic resonance imaging in SEPN1‐related myopathy shows a homogeneous and recognizable pattern

By  

MUSCLE AND NERVE, Vol. 148-639X, Iss. 5, 2015-11 ,pp. : 728-735

John Wiley & Sons Inc

Access to resources Recommend Favorite

Muscle weakness in children with neurofibromatosis type 1

By  

DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY, Vol. 57, Iss. 8, 2015-08 ,pp. : 733-736

John Wiley & Sons Inc

Access to resources Recommend Favorite

Identification of a novel nemaline myopathy‐Causing mutation in the troponin T1 (TNNT1) gene: A case outside of the old order amish

By  

MUSCLE AND NERVE, Vol. 51, Iss. 5, 2015-05 ,pp. : 767-772

John Wiley & Sons Inc

Access to resources Recommend Favorite