NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America

Detalles Bibliográficos
Autores principales: Richard, G, Lauricella, C, Xu, Z, Aksentijevich, I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Oral Presentation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596948/
http://dx.doi.org/10.1186/1546-0096-13-S1-O55
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author Richard, G
Lauricella, C
Xu, Z
Aksentijevich, I
author_facet Richard, G
Lauricella, C
Xu, Z
Aksentijevich, I
author_sort Richard, G
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spelling pubmed-45969482015-10-08 NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America Richard, G Lauricella, C Xu, Z Aksentijevich, I Pediatr Rheumatol Online J Oral Presentation BioMed Central 2015-09-28 /pmc/articles/PMC4596948/ http://dx.doi.org/10.1186/1546-0096-13-S1-O55 Text en Copyright © 2015 Richard et al. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Oral Presentation
Richard, G
Lauricella, C
Xu, Z
Aksentijevich, I
NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title_full NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title_fullStr NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title_full_unstemmed NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title_short NextGen sequencing (NGS) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from North America
title_sort nextgen sequencing (ngs) panel for hereditary recurrent fevers: mutation spectrum, novel mutations, and evidence for re-classification of common variants based on analysis of >3000 cases from north america
topic Oral Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596948/
http://dx.doi.org/10.1186/1546-0096-13-S1-O55
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