Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review

Williams Syndrome (WS) is a rare genetic multisystem disorder that occurs because of a deletion of approximately 25 genes in the 7q11.23 chromosome region. This causes dysmorphic facial appearances, multiple congenital cardiovascular defects, delayed motor skills, and abnormalities in connective tis...

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Detalles Bibliográficos
Autores principales: Çalışkan, Elif, Şahin, Munise Nur, Güldağ, Mahmut Alper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686774/
https://www.ncbi.nlm.nih.gov/pubmed/34970101

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686774/
https://www.ncbi.nlm.nih.gov/pubmed/34970101

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