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TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes
Prader-Willi syndrome (PWS) is a genetic imprinting disease that causes developmental and behavioral disturbances resulting from loss of expression of genes from the paternal chromosome 15q11-q13 region. In about 70% of subjects, this portion of the paternal chromosome is deleted, while 25% have two...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer US
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3164046/ https://ncbi.nlm.nih.gov/pubmed/22127900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11689-010-9051-6 |
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