{
    "record_id": "PubMed.10369869", 
    "reference": {
        "url": "https://www.ncbi.nlm.nih.gov/pubmed/10369869", 
        "type": "PubMed", 
        "id": "10369869"
    }, 
    "title": "A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.", 
    "journal": "Hum. Mol. Genet.", 
    "referenced_glycans": [], 
    "authors": "Munro C.S., Monaco A.P., Maestrini E., Hovnanian A., Calzolari E., Cambiaghi S., Korge B.P., Ocana-Sierra J., Scudder P.M.", 
    "date": "1999", 
    "referenced_proteins": [
        "P29033-1"
    ], 
    "abstract": ""
}