Exome and genome sequencing for inborn errors of immunity

The advent of next generation sequencing (NGS) in 2010 has transformed medicine and particularly the growing field of monogenic inborn errors of immunity, including primary immunodeficiencies (PID). NGS has facilitated the discovery of novel disease-causing genes and the genetic diagnosis of patient...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Allergy Clin Immunol
Päätekijät: Meyts, Isabelle, Bosch, Barbara, Bolze, Alexandre, Boisson, Bertrand, Itan, Yuval, Belkadi, Aziz, Pedergnana, Vincent, Moens, Leen, Picard, Capucine, Cobat, Aurélie, Bossuyt, Xavier, Abel, Laurent, Casanova, Jean-Laurent
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2016
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5074686/
https://ncbi.nlm.nih.gov/pubmed/27720020
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2016.08.003
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