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Figure 1

Figure 1 . From: CDKL5 gene status in female patients with epilepsy and Rett-like features: two new mutations in the catalytic domain.

Complete deletion of exon 10 detected by MLPA (A) and confirmed by cDNA analysis (B).

Hiart Maortua, et al. BMC Med Genet. 2012;13:68-68.

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