Investigation of age-related facial variation among Angelman syndrome patients

Angelman syndrome (AS) is one of the common genetic disorders that could emerge either from a 15q11–q13 deletion or paternal uniparental disomy (UPD) or imprinting or UBE3A mutations. AS comes with various behavioral and phenotypic variability, but the acquisition of subjects for experiment and auto...

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Detalles Bibliográficos
Autores principales: Agbolade, Olalekan, Nazri, Azree, Yaakob, Razali, Ghani, Abdul Azim, Cheah, Yoke Kqueen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531312/
https://www.ncbi.nlm.nih.gov/pubmed/34675349
http://dx.doi.org/10.1038/s41598-021-99944-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531312/
https://www.ncbi.nlm.nih.gov/pubmed/34675349
http://dx.doi.org/10.1038/s41598-021-99944-z

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