Growth Trajectories in Genetic Subtypes of Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the paternal copy of chromosome 15q11-13. The main molecular subtypes of PWS are the deletion of 15q11-13 and non-deletion, and differences in neurobehavioral phenotype are recognized between the subtypes. Th...

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Detalles Bibliográficos
Autores principales: Shepherd, Daisy A., Vos, Niels, Reid, Susan M., Godler, David E., Guzys, Angela, Moreno-Betancur, Margarita, Amor, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397071/
https://www.ncbi.nlm.nih.gov/pubmed/32630716
http://dx.doi.org/10.3390/genes11070736

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397071/
https://www.ncbi.nlm.nih.gov/pubmed/32630716
http://dx.doi.org/10.3390/genes11070736

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