Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family
| Auteurs | Saadi A, Borck G, Boddaert N, Chekkour M C, Imessaoudene B, Munnich A, Colleaux L, Chaouch M |
| Revue | |
| Année | 2 009 |
| Institut | I2BM |