Correspondence on "Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies" by Fountain et al
Genet Med
.
2021 Feb;23(2):421-422.
doi: 10.1038/s41436-020-00978-x.
Epub 2020 Oct 5.
Authors
Anna Paola Capra
1
,
Emanuele Agolini
2
,
Maria Angela La Rosa
1
,
Antonio Novelli
2
,
Silvana Briuglia
3
Affiliations
1
Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Messina, Italy.
2
Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, Rome, Italy.
3
Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Messina, Italy. sbriuglia@unime.it.
PMID:
33012787
DOI:
10.1038/s41436-020-00978-x
No abstract available
Publication types
Letter
Comment
MeSH terms
Humans
Language Development Disorders*
Neurodevelopmental Disorders* / genetics
Ubiquitin-Specific Peptidase 7
Substances
USP7 protein, human
Ubiquitin-Specific Peptidase 7