Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study (Q24622472)

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object named as

Bryan J Traynor

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Dena G. Hernandez

9

object named as

Dena G Hernandez

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author name string

Hannu Laaksovirta

1

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Terhi Peuralinna

2

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Jennifer C Schymick

3

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Shaoi-Lin Lai

5

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Liisa Myllykangas

6

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Raimo Sulkava

7

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Lilja Jansson

8

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J Raphael Gibbs

10

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Michael A Nalls

11

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David Heckerman

12

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Pentti J Tienari

describes a project that uses

13

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language of work or name

English

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publication date

October 2010

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published in

Lancet Neurology

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volume

9

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issue

10

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page(s)

978-85

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genome-wide association study

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A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

inferred from title

cites work

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Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

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Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

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A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

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Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

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Crossref

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970184-8

7 January 2021