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SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

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Figure

Table 1 Clinical findings in LAT1180
Table 2 Major absence-of-heterozygosity regions identified in LAT1180 using SNP array
Table 4 Exome sequencing and filtering strategy inLAT1180¶
Figure 3 Alignment of exome high-throughput sequencing data showingvertical lines SHROOM3 gene mutation c.179G > T bordered by red
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