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. 2017 Sep 4;9(9):1326. doi: 10.15252/emmm.201708209

Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome

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‐Hersh, Eugene Vlodavsky, Liat Appl‐Sarid, Dorit Goldsher, Reuven Bergman, Zvi Segal, Ora Bitterman‐Deutsch, Orly Avni
PMCID: PMC5582371  PMID: 28864777

Abstract

graphic file with name EMMM-9-1326-g001.jpg


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.


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