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Prader–Willi syndrome and autism spectrum disorders: an evolving story
Prader–Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11–q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums,...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer US
2011
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3261277/ https://ncbi.nlm.nih.gov/pubmed/21858456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11689-011-9092-5 |
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