The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes
Deletion of the 16p11.2 CNV affects 25 core genes and is associated with multiple symptoms affecting brain and body, including seizures, hyperactivity,macrocephaly, and obesity. Available data suggest thatmost symptoms are controlled by haploinsufficiency of two or more 16p11.2 genes. To identify in...
| Main Authors: | , , , |
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| Other Authors: | , |
| Format: | Article |
| Language: | English |
| Published: |
Oxford University Press (OUP),
2018-07-10T14:50:13Z.
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| Subjects: | |
| Online Access: | Get fulltext |