Uroporphyrinogen decarboxylase: a splice site mutation causes the deletion of exon 6 in multiple families with porphyria cutanea tarda.

von Garey, J R, Harrison, L M, Franklin, K F, Metcalf, K M, Radisky, E S, Kushner, J P
Veröffentlicht 1990

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes.

von Ajioka, R S, Jorde, L B, Gruen, J R, Yu, P, Dimitrova, D, Barrow, J, Radisky, E, Edwards, C Q, Griffen, L M, Kushner, J P
Veröffentlicht 1997