Exome Sequencing to Identify De Novo Mutations in Sporadic ALS Trios

Nature Neuroscience - United Kingdom
doi 10.1038/nn.3412
Full Text
Abstract

Available in full text

Categories
Neuroscience
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Exome Sequencing of Case-Unaffected-Parents Trios Reveals Recessive and De Novo Genetic Variants in Sporadic ALS

Scientific Reports
Multidisciplinary
2015English

Sporadic Hypertrophic Cardiomyopathy Due to De Novo Myosin Mutations.

Journal of Clinical Investigation
Medicine
1992English

Exome Sequencing to Identify Novel Genes in Hypertension

Circulation: Cardiovascular Genetics
2012English

De Novo Mutations in Sporadic Deletional Duchenne Muscular Dystrophy (DMD) Cases

Experimental & Molecular Medicine
2003English

Using Whole-Exome Sequencing to Identify Variants Inherited From Mosaic Parents

European Journal of Human Genetics
Genetics
2014English

Exome Sequencing Identifies Recurrent Somatic RAC1 Mutations in Melanoma

Nature Genetics
Genetics
2012English

Exome Sequencing Identified New Mutations in a Marfan Syndrome Family

Diagnostic Pathology
Forensic MedicineMedicinePathologyHistology
2014English

Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases

Genomics and Informatics
EvolutionEcologyGeneticsSystematicsHealth InformaticsBehavior
2012English

Preliminary Evaluation of Exome Sequencing to Identify Genetic Markers of Susceptibility to Tuberculosis Disease

BMC Research Notes
BiochemistryMedicineGeneticsMolecular Biology
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy