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A rigorous <i>in silico</i> genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.

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第一作者: Afif,Ben-Mahmoud
第一单位: Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
作者单位: Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar. [1] Department of Laboratory Medicine, Inje University Haeundae Paik Hospital, Busan, South Korea. [2] Department of Cardiovascular Medicine, Cape Fear Valley Medical Center, Fayetteville, NC, United States. [3] Diabetes Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar. [4] Faculdade de Medicina, Unidade de Genética do Instituto da Criança - Hospital das Clínicas HCFMUSP, Universidade de São Paulo, São Paulo, Brazil. [5] School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.;Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil. [6] Inserm UMR 1231 GAD, Genetics of Developmental Disorders, Université de Bourgogne-Franche Comté, Dijon, France.;Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France. [7] UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France. [8] Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, United States.;Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA, United States. [9] Department of Animal Science, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea. [10] Department of Biology, Chungnam National University, Daejeon, South Korea. [11] Department of Biological Sciences, Kent State University, Kent, OH, United States. [12]
DOI 10.3389/fnmol.2022.979061
PMID 36277487
发布时间 2022-10-25
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Frontiers in molecular neuroscience

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