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 |
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| Records Return:
(1)
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| Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
| GM21921 | Male | 15 MO | ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS | GM |
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