Molecular characterization of an allelic series of mutations in the mouse Nox3 gene

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Mammalian Genome, Vol. 22, Iss. 3-4, 2011-04 ,pp. : 156-169

Springer Publishing Company

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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger–Huët anomaly

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Oxford University Press

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The Mottled Mouse as a Model for Human Menkes Disease: Identification of Mutations in the Atp7a Gene

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A novel mouse model of Niemann–Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations

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Novel ENU-induced eye mutations in the mouse: models for human eye disease

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