Reply: Mutations in TUBB4A and spastic paraplegia

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8257|30|13|1858-1859

ISSN： 0885-3185

Source： MOVEMENT DISORDERS, Vol.30, Iss.13, 2015-11, pp. : 1858-1859

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

Mutations in TUBB4A and spastic paraplegia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 13, 2015-11 ,pp. : 1857-1858

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 6, 2015-05 ,pp. : 854-858

John Wiley & Sons Inc

Access to resources Recommend Favorite

H‐ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 6, 2015-05 ,pp. : 828-833

John Wiley & Sons Inc

Access to resources Recommend Favorite

De Novo mutations in the β‐tubulin gene TUBB4: From DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H‐ABC syndrome)

By  

MOVEMENT DISORDERS, Vol. 28, Iss. 10, 2013-09 ,pp. : 1343-1343

John Wiley & Sons Inc

Access to resources Recommend Favorite

Gait outcomes and energy efficiency in patients with hereditary spastic paraplegia

By  

DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY, Vol. 57, Iss. S5, 2015-10 ,pp. : 70-71

John Wiley & Sons Inc

Access to resources Recommend Favorite