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Exploring genome-wide DNA methylation patterns in Aicardi syndrome.
Piras, Ignazio S; Mills, Gabrielle; Llaci, Lorida; Naymik, Marcus; Ramsey, Keri; Belnap, Newell; Balak, Chris D; Jepsen, Wayne M; Szelinger, Szabolcs; Siniard, Ashley L; Lewis, Candace R; LaFleur, Madison; Richholt, Ryan F; De Both, Matt D; Avela, Kristiina; Rangasamy, Sampathkumar; Craig, David W; Narayanan, Vinodh; Järvelä, Irma; Huentelman, Matthew J; Schrauwen, Isabelle.
Afiliación
  • Piras IS; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Mills G; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Llaci L; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Naymik M; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Belnap N; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Balak CD; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Jepsen WM; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Szelinger S; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Siniard AL; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Lewis CR; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • LaFleur M; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Richholt RF; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • De Both MD; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Avela K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Rangasamy S; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Craig DW; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Narayanan V; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Järvelä I; Department of Pathology & Laboratory Medicine, David Geffen School of Medicine, University of California, 10833 Le Conte Ave, Los Angeles, CA 90095, USA.
  • Huentelman MJ; Center for Rare Childhood Disorders, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
  • Schrauwen I; Neurogenomics Division, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ, USA.
Epigenomics ; 9(11): 1373-1386, 2017 11.
Article en En | MEDLINE | ID: mdl-28967789

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Epigénesis Genética / Síndrome de Aicardi Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Epigenomics Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Epigénesis Genética / Síndrome de Aicardi Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Epigenomics Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido