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

Hlady RA, Novakova S, Opavska J, Klinkebiel D, Peters SL, Bies J, Hannah J, Iqbal J, Anderson KM, Siebler HM, Smith LM, Greiner TC, Bastola D, Joshi S, Lockridge O, Simpson MA, Felsher DW, Wagner KU, Chan WC, Christman JK, Opavsky R (2012)
Loss of Dnmt3b function upregulates the tumor modifier Ment and accelerates mouse lymphomagenesis
J Clinical Investigation 122: 163

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