| Title : Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| Author(s) : Harrison V , Connell L , Hayesmoore J , McParland J , Pike MG , Blair E |
| Ref : American Journal of Medicine Genet A , 155A :2826 , 2011 |
| Abstract : |
| PubMedSearch : Harrison_2011_Am.J.Med.Genet.A_155A_2826 |
| PubMedID: 21964664 |