| Title : The Expanding MEGDEL Phenotype: Optic Nerve Atrophy, Microcephaly, and Myoclonic Epilepsy in a Child with SERAC1 Mutations - Lumish_2014_JIMD.Rep_16_75 |
| Author(s) : Lumish HS , Yang Y , Xia F , Wilson A , Chung WK |
| Ref : JIMD Rep , 16 :75 , 2014 |
| Abstract : Lumish_2014_JIMD.Rep_16_75 |
| ESTHER : Lumish_2014_JIMD.Rep_16_75 |
| PubMedSearch : Lumish_2014_JIMD.Rep_16_75 |
| PubMedID: 24997715 |
| Gene_locus related to this paper: human-SERAC1 |
| Gene_locus related to this paper: human-SERAC1 |
Lumish HS, Yang Y, Xia F, Wilson A, Chung WK (2014)
The Expanding MEGDEL Phenotype: Optic Nerve Atrophy, Microcephaly, and Myoclonic Epilepsy in a Child with SERAC1 Mutations
JIMD Rep
16 :75
Lumish HS, Yang Y, Xia F, Wilson A, Chung WK (2014)
JIMD Rep
16 :75