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Human Molecular Genetics
|
February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
Adriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Neuron
|
November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Bradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Nature Genetics
|
July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.
Neuron
|
March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology
|
August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O Johnson, Ruth Chia, Danny E Miller, et al.
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Search research articles
Search
Showing results (251-260 of 255) with videos related to
Sort By:
Page
of 26
You have reached the last page of results.
This site can display upto 255 results.
Human Molecular Genetics
|
February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
Adriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Neuron
|
November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Bradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Nature Genetics
|
July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.
Neuron
|
March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology
|
August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O Johnson, Ruth Chia, Danny E Miller, et al.
Page
of 26