Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2
Open Access
- 1 May 2003
- journal article
- case report
- Published by BMJ in Archives of Disease in Childhood: Fetal & Neonatal
- Vol. 88 (3), 250F-252
- https://doi.org/10.1136/fn.88.3.f250