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. 2014 Mar 13;2(2):204. doi: 10.1002/mgg3.77

Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases

Roberta Spinelli, Alessandra Pirola, Sara Redaelli, Nitesh Sharma, Hima Raman, Simona Valletta, Vera Magistroni, Rocco Piazza, Carlo Gambacorti-Passerini
PMCID: PMC3960063

The original article to which this erratum refers was published in Molecular Genetics and Genomic Medicine 1(4):246–259 (DOI: 10.1002/mgg3.23).

In the published article, there are some errors in the authors' affiliations, which have been corrected in this erratum.

Below is the list of authors showing the corrected affiliations:

Roberta Spinelli1, Alessandra Pirola1, Sara Redaelli1, Nitesh Sharma1, Hima Raman1, Simona Valletta1, Vera Magistroni1, Rocco Piazza1,*, & Carlo Gambacorti-Passerini1,2,*

We regret these errors.

Notes

1

Department of Health Sciences, University of Milano-Bicocca, Monza, Italy

2

Hematology and Clinical Research Unit, San Gerardo Hospital, Monza, Italy

*

Rocco Piazza and Carlo Gambacorti-Passerini served as co-last authors


Articles from Molecular Genetics & Genomic Medicine are provided here courtesy of Blackwell Publishing

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