Further Delineation of Developmental Delay with Gastrointestinal, Cardiovascular, Genitourinary, and Skeletal Abnormalities Caused by <i>ZNF699</i> Gene Mutation

Further Delineation of Developmental Delay with Gastrointestinal, Cardiovascular, Genitourinary, and Skeletal Abnormalities Caused by <i>ZNF699</i> Gene Mutation

Until 2021, the <i>ZNF699</i> gene was not associated with any human genetic disease. There were only two studies exploring the associations between variants in <i>ZNF699</i> and alcohol dependence. In 2021 Bertoli-Avella et al. reported 13 patients with a <i>ZNF699<...

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Bibliographic Details
Main Authors: Mateusz Biela, Malgorzata Rydzanicz, Agnieszka Jankowska, Agnieszka Szlagatys-Sidorkiewicz, Anna Rozensztrauch, Rafał Płoski, Robert Smigiel
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:Genes
Subjects:
<i>ZNF699</i> gene
DEGCAGS syndrome
neurodevelopmental disorder
Online Access:https://www.mdpi.com/2073-4425/13/2/168

Internet

https://www.mdpi.com/2073-4425/13/2/168

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