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Epigenomics Volume 9, 2017 - Issue 11
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Research Article

Exploring genome-wide DNA methylation patterns in Aicardi syndrome

Ignazio S Piras1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Gabrielle Mills1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Lorida Llaci1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Marcus Naymik1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Keri Ramsey1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Newell Belnap1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Chris D Balak1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Wayne M Jepsen1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Szabolcs Szelinger1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;3 Department of Pathology & Laboratory Medicine, David Geffen School of Medicine, University of California, 10833 Le Conte Ave, Los Angeles, CA90095, USAView further author information
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Ashley L Siniard1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Candace R Lewis1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
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Madison LaFleur1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Ryan F Richholt1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Matt D De Both1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
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Kristiina Avela4 Department of Clinical Genetics, Helsinki University Hospital, Meilahdentie 2, FI-00029 Helsinki, FinlandView further author information
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Sampathkumar Rangasamy1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
David W Craig1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;5 University of Southern California, Keck School of Medicine, Department of Translational Genomics, Los Angeles, NRT 1450 Biggy Street, CA90033, USAView further author information
,
Vinodh Narayanan1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
,
Irma Järvelä6 Department of Medical Genetics, University of Helsinki, Haartmaninkatu 8, 00251 Helsinki, FinlandView further author information
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Matthew J Huentelman1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USAView further author information
&
Isabelle Schrauwen1 Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;2 Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA;7 Center for Statistical Genetics, Department of Molecular & Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX77030, USACorrespondence[email protected]
View further author information
 show all
Pages 1373-1386 | Received 28 Apr 2017, Accepted 27 Jul 2017, Published online: 02 Oct 2017

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