Cite
HARVARD Citation
Andersson, E. et al. (n.d.). Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing. Experimental dermatology. 23 (5), pp. 366-368. [Online].
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Andersson, E. et al. (n.d.). Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing. Experimental dermatology. 23 (5), pp. 366-368. [Online].