Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population.

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Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population.

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2014 nî lūn-bûn

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2014年の論文

@ja

2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Genome-wide analysis of CNV (c ...... epsy in a Japanese population.

@en

Genome-wide analysis of CNV

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type

Item

label

Genome-wide analysis of CNV (c ...... epsy in a Japanese population.

@en

Genome-wide analysis of CNV

@nl

prefLabel

Genome-wide analysis of CNV (c ...... epsy in a Japanese population.

@en

Genome-wide analysis of CNV

@nl

P1476

Genome-wide analysis of CNV (c ...... epsy in a Japanese population.

@en

P2093

Aino Nitta

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Asako Koike

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Hiromi Toyoda

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Katsushi Tokunaga

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Kumi Akiyama

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Makoto Honda

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Maria Yamasaki

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

Taku Miyagawa

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

Tsukasa Sasaki

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

Yutaka Honda

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P2860

Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia)

Rare chromosomal deletions and duplications increase risk of schizophrenia

ImmunoChip study implicates antigen presentation to T cells in narcolepsy

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

Functional impact of global rare copy number variation in autism spectrum disorders

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

Narcolepsy is strongly associated with the T-cell receptor alpha locus

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

P2888

jhg.2014.13

P304

235-240

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P31

scholarly article

P356

10.1038/JHG.2014.13

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P433

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

P478

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

P50

Seik-Soon Khor

P577

2014-04-03T00:00:00Z

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P698

24694762

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P921

genome-wide association study

narcolepsy