Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.

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第一作者： Fereshteh,Ashtari

第一单位： Neurology Department, Isfahan Neuroscience Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran ; These authors equally contributed to this work.

作者： Fereshteh,Ashtari ^[1] ; Kioomars,Saliminejad ; Ali,Ahani ; Koorosh,Kamali ; Zhamak,Pahlevanzadeh ; Hamid Reza Khorram,Khorshid

作者单位： Neurology Department, Isfahan Neuroscience Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran ; These authors equally contributed to this work. ^[1]

关键词 Familial Idiopathic Basal Ganglia Calcification Mutation SLC20A2 protein SPP2 protein

PMID 24286000

发布时间 2021-10-21

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Avicenna journal of medical biotechnology

2013年5卷4期

251-6页

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Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.

Avicenna journal of medical biotechnology

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Avicenna journal of medical biotechnology

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Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.

Avicenna journal of medical biotechnology

相似文献

Avicenna journal of medical biotechnology

相关期刊

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