Cortical Myoclonus in a Young Boy with GOSR2 Mutation Mimics Chorea

E-ISSN： 2330-1619|2|1|61-63

ISSN： 2330-1619

Source： MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol.2, Iss.1, 2015-03, pp. : 61-63

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

Adult‐Onset Focal Chorea in Fahr's Disease Resulting From SLC20A2 Mutation: A Novel Phenotype

MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 1, 2015-03 ,pp. : 79-80

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hematologic Follow‐up as Clue to Polycythemia Vera due to JAK2 Mutation Presenting as Late Onset Chorea

MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 5, Iss. 1, 2018-01 ,pp. : 83-85

John Wiley & Sons Inc

Access to resources Recommend Favorite

Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene

MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 3, 2015-09 ,pp. : 271-273

John Wiley & Sons Inc

Access to resources Recommend Favorite

Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome

MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 3, 2015-09 ,pp. : 230-231

John Wiley & Sons Inc

Access to resources Recommend Favorite

Writing Chorea

By Wexler Alice

Rethinking History, Vol. 5, Iss. 3, 2001-11 ,pp. : 421-426

Routledge Ltd

Access to resources Recommend Favorite