Work

Dysregulated COMT Expression in Fragile X Syndrome

Year: 2023

Type: article

Source: NeuroMolecular Medicine

DOI: 10.1007/s12017-023-08754-1

Authors: Kagistia Hana Utami, Nur Amirah Binte Muhammed Yusof, Marta Garcia-Miralles, Niels Henning Skotte, Srikanth Nama, Prabha Sampath, Sarah R. Langley, Mahmoud A. Pouladi

Institutions: Agency for Science, Technology and Research, Nanyang Technological University, University of Freiburg, University of Copenhagen, Novo Nordisk Foundation, Institute of Medical Biology, Duke-NUS Medical School, Genome Institute of Singapore, Cardiff University, University of British Columbia, BC Children's Hospital Research Institute, Djavad Mowafaghian Centre for Brain Health

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: FRAXA Research Foundation, BC Children's Hospital, Michael Smith Health Research BC, Weill Cornell Medical College

OpenAlex ID: W4386537845

FWCI: 0.124

Cites: 28

Cited by: 1

Related to: 10