Biallelic variants in GTF3C3 result in an autosomal recessive intellectual disability

Abstract

Peer reviewed

Kerith-Rae Dias, Anais Begemann, Laura E R Blok, Lachlan De Hayr and See article text for complete list of authors

European Journal of Human Genetics, Vol.31(Supplement 1), pp.7-8

European-Society-of-Human-Genetics (ESHG) Conference, 55th (Vienna, Austria, 11-Jun-2022 - 14-Jun-2022)

2023

Abstract

No abstract available.

Title: Biallelic variants in GTF3C3 result in an autosomal recessive intellectual disability
Authors: Kerith-Rae Dias (Author) - UNSW Sydney
Anais Begemann (Author) - University of Zurich
Laura E R Blok (Author) - Radboud University Medical Center
Lachlan De Hayr (Author) - University of the Sunshine Coast, Queensland, School of Health - Biomedicine
See article text for complete list of authors (Author)
Publication details: European Journal of Human Genetics, Vol.31(Supplement 1), pp.7-8
Conference details: European-Society-of-Human-Genetics (ESHG) Conference, 55th (Vienna, Austria, 11-Jun-2022 - 14-Jun-2022)
Publisher: Nature Publishing Group
DOI: 10.1038/s41431-023-01337-5
ISSN: 1476-5438
Grant note: APP1117394 / NHMRC
Organisation Unit: School of Health - Biomedicine
Language: English
Record Identifier: 99979097602621
Output Type: Abstract

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Collaboration types: Domestic collaboration; International collaboration
Web Of Science research areas: Biochemistry & Molecular Biology; Genetics & Heredity

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