The gene for the muted ( mu ) mouse, a model for Hermansky–Pudlak syndrome, defines a novel protein which regulates vesicle trafficking

By Suzuki T.  

Human Molecular Genetics, Vol. 11, Iss. 6, 2002-03 ,pp. : 697-706

Oxford University Press

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The 3A subunit gene ( Ap3b1 ) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky–Pudlak syndrome and night blindness

By Eicher E.M.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 323-330

Oxford University Press

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The Hermansky–Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomes

By Oh Jangsuk   Liu Zhen-Xiang   Feng Guo Hong   Raposo Graça   Spritz Richard A.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 375-385

Oxford University Press

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Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

By Erway L.C.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 645-653

Oxford University Press

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An Imprinted Mouse Transcript Homologous to the Human Imprinted in Prader-Willi Syndrome ( IPW ) Gene

By Wevrick Rachel   Francke Uta  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 325-332

Oxford University Press

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