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Author Report for: Simpson MA

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    Title: Bi-allelic nonsense mutations inABHD5 underlie a mild phenotype of Dorfman-Chanarin syndrome
    Takeichi T, Sugiura K, Tso S, Simpson MA, McGrath JA, Akiyama M
    Ref: J Dermatol Sci, 81:134, 2016 : PubMed

            

    Title: Loss of Dnmt3b function upregulates the tumor modifier Ment and accelerates mouse lymphomagenesis
    Hlady RA, Novakova S, Opavska J, Klinkebiel D, Peters SL, Bies J, Hannah J, Iqbal J, Anderson KM and Opavsky R <11 more author(s)>
    Ref: J Clinical Investigation, 122:163, 2012 : PubMed

            

    Title: Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia
    Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH
    Ref: American Journal of Human Genetics, 73:1147, 2003 : PubMed

            


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