لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Rodden LN; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.; Oklahoma Center for Neuroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA., Chutake YK; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA., Gilliam K; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA., Lam C; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA., Soragni E; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA., Hauser L; Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Gilliam M; Department of Electrical and Computer Engineering, University of Oklahoma, Norman, OK, USA., Wiley G; Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA., Anderson MP; Department of Biostatistics and Epidemiology, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA., Gottesfeld JM; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA., Lynch DR; Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Bidichandani SI; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.; Oklahoma Center for Neuroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.; Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

المصدر: Human molecular genetics [Hum Mol Genet] 2021 Feb 04; Vol. 29 (23), pp. 3818-3829.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: DNA Methylation* , Epigenesis, Genetic* , Gene Silencing* , Phenotype*, Friedreich Ataxia/*pathology , Leukocytes, Mononuclear/*pathology, Adolescent ; Adult ; Alleles ; Child ; Child, Preschool ; Female ; Friedreich Ataxia/genetics ; Humans ; Infant ; Leukocytes, Mononuclear/metabolism ; Male ; Young Adult