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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Mouse Pale Ear (ep) is Homologous to Human Hermansky-Pudlak Syndrome and Contains a Rare ‘AT-AC’ Intron

By Feng Guo Hong   Bailin Tu   Oh Jangsuk   Spritz Richard A.  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 793-797

Oxford University Press

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A homolog of the human Hermansky-Pudluck syndrome-5 (HPS5) gene is responsible for the oa larval translucent mutants in the silkworm, Bombyx mori

By Fujii T.  

Genetica, Vol. 140, Iss. 10-12, 2012-12 ,pp. : 463-468

Springer Publishing Company

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Characterization of the human HSC20, an unusual DnaJ type III protein, involved in ironsulfur cluster biogenesis

By Uhrigshardt Helge   Singh Anamika   Kovtunovych Gennadiy   Ghosh Manik   Rouault Tracey A.  

Human Molecular Genetics, Vol. 19, Iss. 19, 2010-10 ,pp. : 3816-3834

Oxford University Press

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