A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia

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Human Molecular Genetics, Vol. 12, Iss. 19, 2003-10 ,pp. : 2533-2539

Oxford University Press

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Characterization of lpd (lipid defect): a novel mutation on mouse chromosome 16 associated with a defect in triglyceride metabolism

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Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 743-750

Oxford University Press

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The UTX gene escapes X inactivation in mice and humans

By Willard H.F.  

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Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly

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Molecular Syndromology, Vol. 3, Iss. 1, 2012-06 ,pp. : 25-29

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Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures

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Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1995-1999

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