ADCY5 identified as a novel cause of benign hereditary chorea

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8257|30|13|1726-1726

ISSN： 0885-3185

Source： MOVEMENT DISORDERS, Vol.30, Iss.13, 2015-11, pp. : 1726-1726

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

A de novoADCY5 mutation causes early‐onset autosomal dominant chorea and dystonia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 3, 2015-03 ,pp. : 423-427

John Wiley & Sons Inc

Access to resources Recommend Favorite

Recurrent drop attacks in early childhood as presenting symptom of benign hereditary chorea caused by TITF1 gene mutations

By  

DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY, Vol. 57, Iss. 8, 2015-08 ,pp. : 777-779

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

By  

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

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hereditary Benign Telangiectasia: Two Case Reports

By  

THE JOURNAL OF DERMATOLOGY, Vol. 19, Iss. 6, 1992-06 ,pp. : 384-386

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hereditary benign telangiectasia in monozygotic twins with no family history

By  

INTERNATIONAL JOURNAL OF DERMATOLOGY, Vol. 54, Iss. 4, 2015-04 ,pp. : e95-e96

John Wiley & Sons Inc

Access to resources Recommend Favorite