Genetic risk factors in Finnish patients with Parkinson's disease.

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Genetic risk factors in Finnish patients with Parkinson's disease.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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name

Genetic risk factors in Finnish patients with Parkinson's disease.

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Genetic risk factors in Finnish patients with Parkinson's disease.

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Item

label

Genetic risk factors in Finnish patients with Parkinson's disease.

@en

Genetic risk factors in Finnish patients with Parkinson's disease.

@nl

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Genetic risk factors in Finnish patients with Parkinson's disease.

@en

Genetic risk factors in Finnish patients with Parkinson's disease.

@nl

P1476

Genetic risk factors in Finnish patients with Parkinson's disease.

@en

P2093

Ari Siitonen

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Jaana Autere

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Johanna Eerola-Rautio

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Kari Majamaa

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Michael A Nalls

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Mikko Hiltunen

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Pauli Ylikotila

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Pentti J Tienari

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Raphael Gibbs

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Susanna Ylönen

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A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

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Late onset spinal motor neuronopathy is caused by mutation in CHCHD10.

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39-43

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scholarly article

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10.1016/J.PARKRELDIS.2017.09.021

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P478

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Hilkka Soininen

Andrew Singleton

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2017-09-29T00:00:00Z

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P698

29029963

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P921

Finland

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5812481

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