Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia-Reference-Cited by-同舟云学术

Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia

Published:2013-02-19 Issue:4 Volume:73 Page:546-553
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Hersheson Joshua¹,Mencacci Niccolo E.¹²,Davis Mary¹,MacDonald Nicola³,Trabzuni Daniah¹⁴,Ryten Mina¹,Pittman Alan¹,Paudel Reema¹,Kara Eleanna¹,Fawcett Katherine¹,Plagnol Vincent¹,Bhatia Kailash P.¹,Medlar Alan J.⁵,Stanescu Horia C.⁵,Hardy John¹,Kleta Robert⁵,Wood Nicholas W.¹,Houlden Henry¹

Affiliation:

1. Department of Molecular NeuroscienceUniversity College London Institute of Neurology and National Hospital for Neurology and NeurosurgeryLondon United Kingdom

2. Department of Neurology and Laboratory of NeuroscienceIRCCS Istituto Auxologico ItalianoUniversita degli Studi di Milano Italy

3. Department of Womens Health, UCLHLondon United Kingdom

4. Department of GeneticsKing Faisal Specialist Hospital and Research Centre, PO Box 3354Riyadh 11211 Saudi Arabia

5. Centre for NephrologyUniversity College LondonLondon United Kingdom

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.23832

Reference42 articles.

1. Tolcapone: COMT inhibition for the treatment of Parkinson's disease