A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia

E-ISSN： 1531-8249|80|4|ana.24762-ana.24762

ISSN： 0364-5134

Source： ANNALS OF NEUROLOGY, Vol.80, Iss.4, 2016-10, pp. : n/a-n/a

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

Severe 5,10‐methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia

EUROPEAN JOURNAL OF NEUROLOGY, Vol. 25, Iss. 3, 2018-03 ,pp. : 602-605

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

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

John Wiley & Sons Inc

Access to resources Recommend Favorite

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Cytogenetic and Genome Research, Vol. 152, Iss. 1, 2017-06 ,pp. : 16-21

Karger

Access to resources Recommend Favorite

Gait outcomes and energy efficiency in patients with hereditary spastic paraplegia

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

John Wiley & Sons Inc

Access to resources Recommend Favorite

Functional effects of botulinum toxin type-A treatment and subsequent stretching of spastic calf muscles: A study in patients with hereditary spastic paraplegia

Journal of Rehabilitation Medicine, Vol. 47, Iss. 2, 2015-02 ,pp. : 147-153

Medical Journals Limited

Access to resources Recommend Favorite