Progress in Brain Magnetic Resonance Imaging of Individuals with Prader–Willi Syndrome

Prader–Willi syndrome (PWS), a rare epigenetic disease mapping the imprinted chromosomal domain of 15q11.2-q13.3, manifests a regular neurodevelopmental trajectory in different phases. The current multimodal magnetic resonance imaging (MRI) approach for PWS focues on morphological MRI (mMRI), diffus...

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Detalles Bibliográficos
Autores principales: Huang, Zhongxin, Cai, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917938/
https://www.ncbi.nlm.nih.gov/pubmed/36769704
http://dx.doi.org/10.3390/jcm12031054

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917938/
https://www.ncbi.nlm.nih.gov/pubmed/36769704
http://dx.doi.org/10.3390/jcm12031054

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