{
    "record_id": "PubMed.10051604", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10051604", 
        "type": "PubMed", 
        "id": "10051604"
    }, 
    "title": "Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.", 
    "journal": "Proceedings of the National Academy of Sciences of the United States of America", 
    "referenced_glycans": [], 
    "authors": "Matsuzono Y, Kinoshita N, Tamura S, Shimozawa N, Hamasaki M, Ghaedi K, Wanders RJ, Suzuki Y, Kondo N, Fujiki Y", 
    "date": "1999", 
    "referenced_proteins": [
        "Q9QYU1-1", 
        "P40855-1"
    ], 
    "abstract": ""
}