A 1p31.3 deletion encompassing the nuclear factor 1A gene presenting as possible temporal lobe epilepsy in association with schizoaffective disorder-Reference-Cited by-同舟云学术

A 1p31.3 deletion encompassing the nuclear factor 1A gene presenting as possible temporal lobe epilepsy in association with schizoaffective disorder

Published:2022-07-04 Issue:4 Volume:28 Page:382-387
ISSN:1355-4794
Container-title:Neurocase
language:en
Short-container-title:Neurocase

Author:

Colijn Mark A.¹,Hrynchak Monica²,Hrazdil Chantelle T.³,Willaeys Veerle⁴,White Randall F.⁴⁵,Stowe Robert M.⁶

Affiliation:

1. Department of Psychiatry, The University of Calgary, Calgary, AB, Canada

2. Molecular Cytogenetic Laboratory, Royal Columbian Hospital, The University of British Columbia, New Westminster, BC, Canada

3. Division of Neurology, Department of Medicine, The University of British Columbia, Vancouver, BC, Canada

4. BC Psychosis Program, British Columbia Mental Health & Substance Use Services, Vancouver, BC, Canada

5. Department of Psychiatry, The University of British Columbia, Vancouver, BC, Canada

6. BC Neuropsychiatry Program, Departments of Psychiatry and Neurology (Medicine), and Djavad Mowafaghian Centre for Brain Health, The University of British Columbia, Vancouver, BC, Canada

Funder

no funding

Publisher

Informa UK Limited

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Link

https://www.tandfonline.com/doi/pdf/10.1080/13554794.2022.2132869

Reference44 articles.

1. Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA gene

2. Quantitative Analysis of Interictal Behavior in Temporal Lobe Epilepsy

3. Calcium signalling and psychiatric disease: bipolar disorder and schizophrenia

4. Interstitial microdeletion of chromosome 1p in two siblings

5. Differential neuronal and glial expression of nuclear factor I proteins in the cerebral cortex of adult mice

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