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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Detalles Bibliográficos
Autores principales: Henkhaus, Rebecca S., Bittel, Douglas C., Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164046/
https://www.ncbi.nlm.nih.gov/pubmed/22127900
http://dx.doi.org/10.1007/s11689-010-9051-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164046/
https://www.ncbi.nlm.nih.gov/pubmed/22127900
http://dx.doi.org/10.1007/s11689-010-9051-6

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