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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...
Autores principales: | Huang, Zhongxin, Cai, Jinhua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
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 |
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