A familial case of PDE10A ‐associated childhood‐onset chorea with bilateral striatal lesions-Reference-Cited by-同舟云学术

A familial case of PDE10A ‐associated childhood‐onset chorea with bilateral striatal lesions

Published:2017-11-22 Issue:1 Volume:33 Page:177-179
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Miyatake Satoko¹²,Koshimizu Eriko¹,Shirai Ikuko³,Kumada Satoko³,Nakata Yasuhiro⁴,Kamemaru Aiko¹,Nakashima Mitsuko¹⁵,Mizuguchi Takeshi¹,Miyake Noriko¹,Saitsu Hirotomo¹⁵,Matsumoto Naomichi¹

Affiliation:

1. Department of Human GeneticsYokohama City University Graduate School of MedicineYokohama Kanagawa Japan

2. Clinical Genetics DepartmentYokohama City University HospitalYokohama Kanagawa Japan

3. Department of NeuropediatricsTokyo Metropolitan Neurological HospitalFuchu Tokyo Japan

4. Department of NeuroradiologyTokyo Metropolitan Neurological HospitalFuchu Tokyo Japan

5. Department of BiochemistryHamamatsu University School of MedicineShizuoka Japan

Funder

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Ministry of Health, Labour and Welfare

Ichiro Kanehara Foundation

Takeda Science Foundation

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27219

Reference7 articles.

1. Benign hereditary chorea

2. Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

4. De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

5. PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder

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