Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment

Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder characterized by varying degrees of intellectual disability, severely delayed language development and specific facial features, and is caused by a deletion within chromosome 22q13.3. SHANK3, which is located at the terminal end of this...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Ziats, Catherine A., Grosvenor, Luke P., Sarasua, Sara M., Thurm, Audrey E., Swedo, Susan E., Mahfouz, Ahmed, Rennert, Owen M., Ziats, Mark N.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2019
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6420160/
https://ncbi.nlm.nih.gov/pubmed/30875393
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0213921
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