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Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome.

Clayton, PT; Kalter, DC; Atherton, DJ; Besley, GT; Broadhead, DM; (1989) Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome. J Inherit Metab Dis , 12 Sup pp. 358-360.

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Type: Article
Title: Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome.
Location: United States
Keywords: Acyltransferases, Cells, Cultured, Chondrodysplasia Punctata, Female, Fibroblasts, Genes, Dominant, Humans, Infant, Male, Microbodies, Reference Values, Skin, X Chromosome
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health > ICH Genetics and Genomic Medicine Prog
URI: http://discovery.ucl.ac.uk/id/eprint/1349758
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