Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.,Genetics in Medicine

当前位置： X-MOL 学术 › Genet. Med. › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.
Genetics in Medicine ( IF 8.8 ) Pub Date : 2019-Jan-14 , DOI: 10.1038/s41436-018-0413-x
Bettina E Mucha ₁ , Siddharth Banka ₂ , Norbert Fonya Ajeawung ₃ , Sirinart Molidperee ₃ , Gary G Chen ₄ , Mary Kay Koenig ₅ , Rhamat B Adejumo ₅ , Marianne Till ₆ , Michael Harbord ₇ , Renee Perrier ₈ , Emmanuelle Lemyre ₉ , Renee-Myriam Boucher ₁₀ , Brian G Skotko ₁₁ , Jessica L Waxler ₁₁ , Mary Ann Thomas ₈ , Jennelle C Hodge ₁₂ , Jozef Gecz ₁₃ , Jillian Nicholl ₁₄ , Lesley McGregor ₁₄ , Tobias Linden ₁₅ , Sanjay M Sisodiya _{16,

17} , Damien Sanlaville ₆ , Sau W Cheung ₁₈ , Carl Ernst ₄ , Philippe M Campeau ₉

Affiliation

Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada.
Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, M13 9PL, Manchester, UK.
Centre de Recherche du CHU Sainte-Justine, Montreal, QC, Canada.
Department of Psychiatry, McGill University, Montreal, QC, Canada.
Department of Pediatrics, Division of Child & Adolescent Neurology, The University of Texas McGovern Medical School, Houston, TX, USA.
Service de Génétique CHU de Lyon-GH Est, Lyon, France.
Department of Pediatrics, Flinders Medical Centre, Bedford Park, SA, Australia.
Department of Medical Genetics, University of Calgary, Calgary, AB, Canada.
Department of Pediatrics, Université de Montréal, Montreal, QC, Canada.
Department of Pediatrics, CHU Laval, Quebec City, QC, Canada.
Division of Medical Genetics, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Adelaide Medical School and Robinson Research Institute, The University of Adelaide, Adelaide, Australia.
South Australian Clinical Genetics Service, SA Pathology, Women's and Children's Hospital, Adelaide, Australia.
Klinik für Neuropädiatrie und Stoffwechselerkrankungen, Zentrum für Kinder- und Jugendmedizin, Oldenburg, Germany.
Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, United Kingdom.
Chalfont Centre for Epilepsy, Bucks, United Kingdom.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

The original version of this Article contained an error in the spelling of the author Siddharth Banka, which was incorrectly given as Siddhart Banka. This has now been corrected in both the PDF and HTML versions of the Article.

中文翻译：