{
    "record_id": "PubMed.10364682", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10364682", 
        "type": "PubMed", 
        "id": "10364682"
    }, 
    "title": "Mutation analysis in patients with congenital adrenal hyperplasia in the Spanish population: identification of putative novel steroid 21-hydroxylase deficiency alleles associated with the classic form of the disease.", 
    "journal": "Hum. Hered.", 
    "referenced_glycans": [], 
    "authors": "Tusie-Luna M.T., Lobato M.N., Meseguer A., Ordonez-Sanchez M.L.", 
    "date": "1999", 
    "referenced_proteins": [
        "P08686-1"
    ], 
    "abstract": ""
}