Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease.Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson's disease risks.

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Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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2015 nî lūn-bûn

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Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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P1476

Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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Lan Cheng

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Ling Wang

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Nan-Nan Li

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Rong Peng

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Wen-Juan Yu

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Xiao-Yi Sun

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P2860

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Substitution p.A350V in Na⁺/Mg²⁺ exchanger SLC41A1, potentially associated with Parkinson's disease, is a gain-of-function mutation

SLC41A1 is a novel mammalian Mg2+ carrier

Human gene SLC41A1 encodes for the Na+/Mg²+ exchanger

The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Epidemiology of Parkinson's disease

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

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706-711

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scholarly article

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10.1002/AJMG.B.32365

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168

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2015-08-26T00:00:00Z

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P698

26308152

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Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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P2860

P2860

Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698