SCL20A2 mutation presenting with acute ischemic stroke: a case report.

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SCL20A2 mutation presenting with acute ischemic stroke: a case report.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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SCL20A2 mutation presenting with acute ischemic stroke: a case report.

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SCL20A2 mutation presenting with acute ischemic stroke: a case report.

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SCL20A2 mutation presenting with acute ischemic stroke: a case report.

@en

SCL20A2 mutation presenting with acute ischemic stroke: a case report.

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SCL20A2 mutation presenting with acute ischemic stroke: a case report.

@en

SCL20A2 mutation presenting with acute ischemic stroke: a case report.

@nl

P1476

SCL20A2 mutation presenting with acute ischemic stroke: a case report.

@en

P2093

Gaoting Ma

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Meijia Zhu

http://www.w3.org/2001/XMLSchema#string

Xiaoyu Zhang

http://www.w3.org/2001/XMLSchema#string

Zhangning Zhao

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P2860

Subacute dementia and imaging correlates in a case of Fahr's disease

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

Ischemic stroke in a young patient with Fahr's disease: a case report.

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

Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterization.

Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes.

PDGF, pericytes and the pathogenesis of idiopathic basal ganglia calcification (IBGC).

Fahr's Disease Presenting with Aneurysmal Subarachnoid Hemorrhage.

Microangiopathy in primary familial brain calcification: Evidence from skin biopsies.

Primary familial brain calcification: update on molecular genetics.

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s12883-018-1012-9

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scholarly article

case report

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10.1186/S12883-018-1012-9

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2018-01-19T00:00:00Z

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1100484908

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29351787

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