Corrigendum to: Sequence variation in PPP1R13L results in a novel form of cardio-cutaneous syndrome (EMBO Molecular Medicine, (2017), 9, 3, (319-336), 10.15252/emmm.201606523)

Tzipora C. Falik-Zaccai, Yiftah Barsheshet, Hanna Mandel, Meital Segev, Avraham Lorber, Shachaf Gelberg, Limor Kalfon, Shani Ben Haroush, Adel Shalata, Liat Gelernter-Yaniv, Sarah Chaim, Dorith Raviv Shay, Morad Khayat, Michal Werbner, Inbar Levi, Yishay Shoval, Galit Tal, Stavit Shalev, Eli Reuveni, Emily Avitan-HershEugene Vlodavsky, Liat Appl-Sarid, Dorit Goldsher, Reuven Bergman, Zvi Segal, Ora Bitterman-Deutsch, Orly Avni

Research output: Contribution to journalComment/debate

5 Scopus citations

Abstract

The accession numbers for the reported data were inadvertently omitted. The authors apologize for this oversight and any inconvenience caused, and hereby provide the missing information: The raw and processed data are all available at ArrayExpress (http://www.ebi.ac.uk/arrayexpress/) under the accession numbers:E-MTAB-5812 (for the results from the 7- and 12-week-old mice and for the in vivo treatment with LPS), and E-MTAB-5826 (for the results from the knocked down cardiomyocytes). The accession number for the causative sequence variation is available at ClinVar (https://www. ncbi.nlm.nih.gov/clinvar/) under accession number SCV000579451.

Original languageEnglish
Pages (from-to)1326
Number of pages1
JournalEMBO Molecular Medicine
Volume9
Issue number9
DOIs
StatePublished - Sep 2017

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