GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition.

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第一作者： Hanan E,Shamseldin

第一单位： Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia.

作者： Hanan E,Shamseldin ^[1] ; Ikuo,Masuho ^[2] ; Ahmed,Alenizi ^[3] ; Suad,Alyamani ^[4] ; Dipak N,Patil ^[2] ; Niema,Ibrahim ^[1] ; Kirill A,Martemyanov ^[5] ; Fowzan S,Alkuraya ^[6]

作者单位： Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia. ^[1] Department of Neuroscience, The Scripps Research Institute, 130 Scripps Way, #3C2, Jupiter, FL, 33458, USA. ^[2] Department of Pediatrics, King Saud Medical City, Riyadh, Saudi Arabia. ^[3] Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. ^[4] Department of Neuroscience, The Scripps Research Institute, 130 Scripps Way, #3C2, Jupiter, FL, 33458, USA. Kirill@scripps.edu. ^[5] Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia. falkuraya@kfshrc.edu.sa. ^[6] Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa. ^[7]

关键词 Attention deficit hyperactivity disorder (ADHD)G protein coupled receptors (GPCR)Hippocampus Linkage Mendelian Neuropsychiatric disorders Striatum

DOI 10.1186/s13059-016-1061-6

PMID 27677260

发布时间 2019-11-20

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