Nature Genetics
36, 1219 - 1224 (2004)
Published online: 24 October 2004; | doi:10.1038/ng1458
X-linked inheritance of Fanconi anemia complementation group BAmom Ruhikanta Meetei, Marieke Levitus, Yutong Xue, Annette L Medhurst, Michel Zwaan, Chen Ling, Martin A Rooimans, Patrick Bier, Maureen Hoatlin, Gerard Pals, Johan P de Winter, Weidong Wang
& Hans JoenjeSupplementary Fig. 1 (pdf 320K)
Human and mouse FANCB proteins contain a nuclear-localization sequence near the C-terminus. Supplementary Fig. 2 (pdf 32K)
A control experiment for FANCA-dependent nuclear localization of FAAp95. Supplementary Fig. 3 (pdf 32K)
FAAP95 cDNA partially complemented the HSC230 cell line for its MMC-hypersensitivity. Supplementary Fig. 4 (pdf 32K)
FANCB is subject to X inactivation which is skewed towards the mutated allele in heterozygous FANCB mutation carriers. Supplementary Table 1 (pdf 32K)
Clinical symptoms of 4 FA-B patients.
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