Identification of SLC20A2 deletions in patients with primary familial brain calcification-Reference-Cited by-同舟云学术

Identification of SLC20A2 deletions in patients with primary familial brain calcification

Published:2019-04-25 Issue:1 Volume:96 Page:53-60
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Guo Xin‐Xin¹,Su Hui‐Zhen¹,Zou Xiao‐Huan¹,Lai Lu‐Lu¹,Lu Ying‐Qian¹,Wang Chong¹,Li Yun‐Lu¹,Hong Jing‐Mei¹,Zhao Miao¹,Lin Kun‐Xin¹,Lin Jie¹,Zeng Yi‐Heng¹,Yao Xiang‐Ping¹,Wang Ning¹²^ORCID,Chen Wan‐Jin¹²^ORCID

Affiliation:

1. Department of Neurology and Institute of NeurologyThe First Affiliated Hospital of Fujian Medical University Fuzhou China

2. Fujian Key Laboratory of Molecular Neurology, Fujian Medical University Fuzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13540

Reference42 articles.

1. What is and what is not ‘Fahr's disease’

2. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

3. Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

4. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

5. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification

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