Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing-Reference-Cited by-同舟云学术

Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing

Published:2013-02-28 Issue:2 Volume:8 Page:e56599
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Grillo Elisa,Lo Rizzo Caterina,Bianciardi Laura,Bizzarri Veronica,Baldassarri Margherita,Spiga Ottavia,Furini Simone,De Felice Claudio,Signorini Cinzia,Leoncini Silvia,Pecorelli Alessandra,Ciccoli Lucia,Mencarelli Maria Antonietta,Hayek Joussef,Meloni Ilaria,Ariani Francesca,Mari Francesca,Renieri Alessandra

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference35 articles.

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3. Preserved speech variants of the Rett syndrome: molecular and clinical analysis;M Zappella;Am J Med Genet,2001

4. Investigating genotype-phenotype relationships in Rett syndrome using an international data set;A Bebbington;Neurology,2008

5. Investigation of modifier genes within copy number variations in Rett syndrome;R Artuso;J Hum Genet,2011

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