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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4437632

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

About this item

Full title

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Publisher

United States: American Association for the Advancement of Science

Journal title

Science (American Association for the Advancement of Science), 2015-03, Vol.347 (6229), p.1436-1441

Language

English

Formats

Publication information

Publisher

United States: American Association for the Advancement of Science

More information

Scope and Contents

Contents

Amyotrophic lateral sclerosis (ALS) is a devastating neurological disease with no effective treatment. We report the results of a moderate-scale sequencing study aimed at increasing the number of genes known to contribute to predisposition for ALS. We performed whole-exome sequencing of 2869 ALS patients and 6405 controls. Several known ALS genes w...

Alternative Titles

Full title

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4437632

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4437632

Other Identifiers

ISSN

0036-8075

E-ISSN

1095-9203

DOI

10.1126/science.aaa3650

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