ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients-Reference-Cited by-同舟云学术

ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients

Published:2017-08 Issue: Volume:41 Page:37-43
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Carecchio Miryam^ORCID,Mencacci Niccolò E.,Iodice Alessandro,Pons Roser,Panteghini Celeste,Zorzi Giovanna,Zibordi Federica^ORCID,Bonakis Anastasios,Dinopoulos Argyris,Jankovic Joseph,Stefanis Leonidas,Bhatia Kailash P.,Monti Valentina,R'Bibo Lea^ORCID,Veneziano Liana,Garavaglia Barbara,Fusco Carlo,Wood Nicholas,Stamelou Maria,Nardocci Nardo

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference18 articles.

1. Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5;Chen;Arch. Neurol.,2012

2. Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder;Fernandez;Ann. Neurol.,2001

3. Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia;Chen;Ann. Neurol.,2014

4. ADCY5 mutations are another cause of benign hereditary chorea;Mencacci;Neurology,2015

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