Publication

Schüle B, Armstrong DD, Vogel H, Oviedo A, and Francke U. , Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure. Clin Genet74(2):116-126 2008
PubMed ID: 18477000

Records Return:  (1) Show
 
Catalog IDGenderAge at SamplingDescription
GM21921Male15 MOENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS