Monoamine oxidase A activity in fibroblasts as a functional confirmation of MAOA variants-Reference-Cited by-同舟云学术

Monoamine oxidase A activity in fibroblasts as a functional confirmation of MAOA variants

Published:2020-12-28 Issue:1 Volume:58 Page:114-121
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Peters Tessa M. A.¹²^ORCID,Lammerts van Bueren Irma²,Geurtz Ben P.B.H.²,Coene Karlien L. M.²,Leeuw Nicole³,Brunner Han G.³⁴⁵⁶,Jónsson Jón J.⁷⁸,Willemsen Michèl A. A. P.⁹,Wevers Ron A.²,Verbeek Marcel M.¹²

Affiliation:

1. Department of Neurology Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center Nijmegen The Netherlands

2. Department of Laboratory Medicine, Translational Metabolic Laboratory (TML) Radboud University Medical Center Nijmegen The Netherlands

3. Department of Human Genetics and Donders Centre for Cognitive Neuroscience Radboud University Medical Center Nijmegen The Netherlands

4. Department of Clinical Genetics Maastricht University Medical Center+ Maastricht The Netherlands

5. Department of Genetics and Cell Biology Maastricht University Medical Center+ Maastricht The Netherlands

6. GROW Institute for Developmental Biology and Cancer Maastricht University Medical Centre Maastricht The Netherlands

7. Department of Genetics and Molecular Medicine Landspitali University Hospital Reykjavik Iceland

8. Department of Biochemistry and Molecular Biology, Faculty of Medicine University of Iceland Reykjavik Iceland

9. Department of Pediatric Neurology Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center Nijmegen The Netherlands

Funder

Association for Progressive Communications

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12194

Reference21 articles.

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2. Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

3. Monoamine oxidase deficiency: a cause of flushing and attention‐deficit/hyperactivity disorder?;Cheung NW;Arch Intern Med,2001

4. 20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

5. New insights into Brunner syndrome and potential for targeted therapy

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