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

Shamseldin, Hanan E; Masuho, Ikuo; Alenizi, Ahmed; Alyamani, Suad; Patil, Dipak N; Ibrahim, Niema; Martemyanov, Kirill A; Alkuraya, Fowzan S

Shamseldin, Hanan E; Masuho, Ikuo; Alenizi, Ahmed; Alyamani, Suad; Patil, Dipak N; Ibrahim, Niema; Martemyanov, Kirill A; Alkuraya, Fowzan S.

Afiliação

Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia.
Masuho I; Department of Neuroscience, The Scripps Research Institute, 130 Scripps Way, #3C2, Jupiter, FL, 33458, USA.
Alenizi A; Department of Pediatrics, King Saud Medical City, Riyadh, Saudi Arabia.
Alyamani S; Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Patil DN; Department of Neuroscience, The Scripps Research Institute, 130 Scripps Way, #3C2, Jupiter, FL, 33458, USA.
Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia.
Martemyanov KA; Department of Neuroscience, The Scripps Research Institute, 130 Scripps Way, #3C2, Jupiter, FL, 33458, USA. Kirill@scripps.edu.
Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh, 11211, Saudi Arabia. falkuraya@kfshrc.edu.sa.

Genome Biol ; 17(1): 195, 2016 Sep 27.

Article em En | MEDLINE | ID: mdl-27677260

Palavras-chave

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

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: Genome Biol Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Arábia Saudita

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