Fahr's Disease Linked to a Novel <b><i>SLC20A2 </i></b>Gene Mutation Manifesting with Dynamic Aphasia-Reference-Cited by-同舟云学术

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Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia

Published:2014 Issue:3 Volume:14 Page:133-138
ISSN:1660-2854
Container-title:Neurodegenerative Diseases
language:en
Short-container-title:Neurodegener Dis

Author:

Brighina Laura,Saracchi Enrico,Ferri Francesca,Gagliardi Monica,Tarantino Patrizia,Morzenti Sabrina,Musarra Monica,Patassini Mirko,Annesi Grazia,Ferrarese Carlo

Publisher

S. Karger AG

Subject

Clinical Neurology,Neurology

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Genetics of Primary Familial Brain Calcification: A Literature Review;International Journal of Molecular Sciences;2023-06-29

2. Brain Calcifications: Genetic, Molecular, and Clinical Aspects;International Journal of Molecular Sciences;2023-05-19

3. Fahr’s disease with an initial presentation of crescendo TIA;BMJ Case Reports;2021-06

4. Cortical myoclonus and epilepsy in a family with a new SLC20A2 mutation;Journal of Neurology;2020-04-09

5. Novel SLC20A2 mutation in primary familial brain calcification with disturbance of sustained phonation and orofacial apraxia;Journal of the Neurological Sciences;2018-07

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