A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations-Reference-Cited by-同舟云学术

A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations

Published:2017-09-26 Issue:11 Volume:32 Page:1646-1647
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Esposito Silvia¹,Carecchio Miryam¹²³,Tonduti Davide¹,Saletti Veronica¹,Panteghini Celeste²,Chiapparini Luisa⁴,Zorzi Giovanna¹,Pantaleoni Chiara¹,Garavaglia Barbara²,Krainc Dimitri⁵,Lubbe Steven J.⁵,Nardocci Nardo¹,Mencacci Niccolò E.⁵

Affiliation:

1. Department of Paediatric Neuroscience; IRCCS Foundation Carlo Besta Neurological Institute; Milan Italy

2. Molecular Neurogenetics Unit; IRCCS Foundation Carlo Besta Neurological Institute; Milan Italy

3. Department of Medicine and Surgery; PhD Programme in Molecular and Translational Medicine, Milan Bicocca University; Monza Italy

4. Neuroradiology Department; IRCCS Foundation Carlo Besta Neurological Institute; Milan Italy

5. Department of Neurology; Northwestern University, Feinberg School of Medicine; Chicago Illinois USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference5 articles.

1. De novo mutations in PDE10A cause childhood-onset chorea with bilateral striatal lesions;Mencacci;Am J Hum Genet,2015

2. Biallelic mutations in PDE10A lead to loss of striatal PDE10A and a hyperkinetic movement disorder with onset in infancy;Diggle;Am J Hum Genet,2015

3. Neurological disorders associated with striatal lesions: classification and diagnostic approach;Tonduti;Curr Neurol Neurosci Rep,2016

5. Clinical spectrum of dopa-responsive dystonia and related disorders;Lee;Curr Neurol Neurosci Rep,2014

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