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Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome
BACKGROUND: Prader–Willi syndrome (PWS) is a complex neurogenetic disorder with symptoms that indicate not only hypothalamic, but also a global, central nervous system (CNS) dysfunction. However, little is known about developmental differences in brain structure in children with PWS. Thus, our aim w...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4015928/ https://ncbi.nlm.nih.gov/pubmed/24144356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-5-31 |
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