{
    "PMID": "10439241",
    "TI": "Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families.",
    "JT": "Experimental dermatology",
    "BTI": "",
    "DP": "1999-08",
    "AU": "Korge B P, Healy E, Traupe H, P\u00fcnter C, Mauch C, Hamm H, Birch-Machin M A, Belgaid C E, Stephenson A M, Holmes S C, Darlington S, Messenger A G, Rees J L, Munro C S"
}
