Association of IMMP2L deletion with neurodevelopmental disorders: new case report and review of the literature.
The inner mitochondrial membrane peptidase subunit 2-like protein, the IMMP2L gene in 7q31.1, have been associated with different neurodevelopmental disorders, including autism spectrum disorders, attention deficit/hyperactivity disorder and Gilles de la Tourette's syndrome (GTS). Since the use...
-д хадгалсан:
| Үндсэн зохиолчид: | , , , , , |
|---|---|
| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
Discover STM Publishing Ltd
2023-02-01
|
| Цуврал: | Journal of Biochemical and Clinical Genetics |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://www.jbcgenetics.com/?mno=134094 |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
|