{
    "record_id": "PubMed.10545596", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10545596", 
        "type": "PubMed", 
        "id": "10545596"
    }, 
    "title": "Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1.", 
    "journal": "Hum. Mol. Genet.", 
    "referenced_glycans": [], 
    "authors": "Letarte M., Marchuk D.A., Pece-Barbara N., Vera S., Cymerman U.", 
    "date": "1999", 
    "referenced_proteins": [
        "P17813-1"
    ], 
    "abstract": ""
}