{
    "record_id": "PubMed.10508514", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10508514", 
        "type": "PubMed", 
        "id": "10508514"
    }, 
    "title": "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.", 
    "journal": "Nat. Genet.", 
    "referenced_glycans": [], 
    "authors": "Francke U., Wan M., Zoghbi H.Y., Amir R.E., Tran C.Q., Van den Veyver I.B.", 
    "date": "1999", 
    "referenced_proteins": [
        "P51608-1"
    ], 
    "abstract": ""
}