Phelan-McDermid Syndrome, Autism, and SHANK3
Автор: Rare Disease Report
Загружено: 2014-11-18
Просмотров: 8475
Описание:
Phelan-McDermid syndrome is a genetic syndrome caused by disruption of the SHANK3/ProSAP2 gene on the terminal end of chromosome 22. There is a wide range of symptoms in children with Phelan-McDermid syndrome but it has many similarities to autism. It is hopeful that much of the research in Phelan-McDermid syndrome and SHANK3 mutations will not only help children with Phelan-McDermid syndrome but also those with autism.
In this interview, Alexander Kolevzon, MD of the Seaver Autism Center at Mount Sinai Hospital talks about the SHANK3 gene and its importance to our understanding of Phelan-McDermid syndrome and possibly autism.
Повторяем попытку...
Доступные форматы для скачивания:
Скачать видео
-
Информация по загрузке:
