Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification-Reference-Cited by-同舟云学术

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Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification

Published:2013-02-14 Issue:3 Volume:20 Page:
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Lemos R. R.¹,Oliveira M. F.²,Oliveira J. R. M.¹³

Affiliation:

1. Keizo Asami Laboratory (LIKA) Federal University of Pernambuco (UFPE) Recife PEBrazil

2. Neurosurgery residency program Hospital do Servidor Público Estadual de São Paulo São Paulo SPBrazil

3. Neuropsychiatric Department Federal University of Pernambuco (UFPE) Recife PE Brazil

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.12044

Reference7 articles.

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

2. A young woman with visual hallucinations, delusions of persecution and a history of performing arson with possible three-generation Fahr disease

3. Anticipation of Familial Idiopathic Basal Ganglia Calcification?

4. Updating Genetic Studies in Familial Idiopathic Basal Ganglia Calcification

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

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

4. The biology of vascular calcification;International Review of Cell and Molecular Biology;2020

5. Lack of Major Ophthalmic Findings in Patients with Primary Familial Brain Calcification Linked to SLC20A2 and PDGFB;Journal of Molecular Neuroscience;2019-01-03

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