H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?-Reference-Cited by-同舟云学术

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

Published:2014-12-27 Issue:6 Volume:30 Page:828-833
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Erro Roberto¹²,Hersheson Joshua³,Ganos Christos¹⁴,Mencacci Niccoló E.³,Stamelou Maria¹⁵⁶,Batla Amit¹,Thust Stefanie Catherine⁷,Bras Jose M.³,Guerreiro Rita J.³,Hardy John³,Quinn Niall P.¹,Houlden Henry³,Bhatia Kailash P.¹

Affiliation:

1. Sobell Department of Motor Neuroscience and Movement Disorders; University College London (UCL) Institute of Neurology; London United Kingdom

2. Dipartimento di Scienze Neurologiche e del Movimento; Università di Verona; Verona Italy

3. Department of Molecular Neuroscience; UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery; London United Kingdom

4. University Medical Center Hamburg-Eppendorf (UKE); Neurology Hamburg Germany

5. Second Department of Neurology; Kapodistrian University of Athens; Greece

6. Neurology Clinic; Philipps University; Marburg Germany

7. The Lysholm Department of Neuroradiology; National Hospital for Neurology and Neurosurgery; London United Kingdom

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.26129/fullpdf

Reference19 articles.

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4. Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation;Hamilton;Brain,2014

5. Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies;Miyatake;Neurology,2014

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