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

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

Descripción completa

Detalles Bibliográficos
Autores principales: Biela, Mateusz, Rydzanicz, Malgorzata, Jankowska, Agnieszka, Szlagatys-Sidorkiewicz, Agnieszka, Rozensztrauch, Anna, Płoski, Rafał, Smigiel, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872584/
https://www.ncbi.nlm.nih.gov/pubmed/35205213
http://dx.doi.org/10.3390/genes13020168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872584/
https://www.ncbi.nlm.nih.gov/pubmed/35205213
http://dx.doi.org/10.3390/genes13020168

Ejemplares similares