Psychiatric phenotypes associated with hyperprolinemia: A systematic review-Reference-Cited by-同舟云学术

Psychiatric phenotypes associated with hyperprolinemia: A systematic review

Published:2021-07 Issue:5 Volume:186 Page:289-317
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Namavar Yasmin¹²^ORCID,Duineveld Denise Joanne¹,Both Geertje Ingena Angelique¹,Fiksinski Ania Maria¹³⁴,Vorstman Jacob Abraham Schrey⁵⁶⁷,Verhoeven‐Duif Nanda Margriet⁸,Zinkstok Janneke Rozemarijn¹

Affiliation:

1. Department of Psychiatry and Brain Center University Medical Center Utrecht Utrecht The Netherlands

2. Department of Psychiatry Amsterdam UMC Location AMC Amsterdam The Netherlands

3. Clinical Genetics Research Program Centre for Addiction and Mental Health Toronto Ontario Canada

4. The Dalglish Family 22q Clinic for 22q11.2 Deletion Syndrome Toronto General Hospital, University Health Network Toronto Ontario Canada

5. Program in Genetics and Genome Biology Research Institute Toronto Ontario Canada

6. Department of Psychiatry The Hospital for Sick Children Toronto Ontario Canada

7. Department of Psychiatry University of Toronto Toronto Ontario Canada

8. Section of Metabolic Diagnostics, Department of Genetics University Medical Center Utrecht, Utrecht University Utrecht The Netherlands

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32869

Reference64 articles.

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2. Avdjieva‐Tzavella D. Kahtom H. Ivanova M. Delchev T.&Tincheva R.(2019). Autism spectrum disorder as a presentation of hyperprolinemia. Paper presented at the Society for the study of inborn errors of metabolism Rotterdam the Netherlands.

3. Measurement of Glutamate and Glutamine in the Medial Prefrontal Cortex of Never-Treated Schizophrenic Patients and Healthy Controls by Proton Magnetic Resonance Spectroscopy

4. Functional Consequences of PRODH Missense Mutations

5. Disrupted Dopaminergic Neurotransmission in 22q11 Deletion Syndrome

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