The int22h1/int22h2-Mediated Xq28 Duplication Syndrome: An Intersection between Neurodevelopment, Immunology, and Cancer

The int22h1/int22h2-mediated Xq28 duplication syndrome is a rare X-linked intellectual disability syndrome (XLIDS) arising from a duplication of the segment between intron 22 homologous regions 1 and 2, on the q28 subregion of the X chromosome. The main clinical features of the syndrome include inte...

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Detalles Bibliográficos
Autores principales: Ballout, Rami A., El-Hattab, Ayman W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229372/
https://www.ncbi.nlm.nih.gov/pubmed/34199727
http://dx.doi.org/10.3390/genes12060860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229372/
https://www.ncbi.nlm.nih.gov/pubmed/34199727
http://dx.doi.org/10.3390/genes12060860

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