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Figure 6 | Orphanet Journal of Rare Diseases

Figure 6

From: The diagnosis of inherited metabolic diseases by microarray gene expression profiling

Figure 6

Genes identified with premature termination codon mutations leading to nonsense mediated decay. Messenger RNA expression levels for all patients for selected genes are shown. The outliers seen at the bottom of distribution correspond to patients (numbered) with nonsense mediated decay associated mutations. The genes ACADM, GAA and MOCS2 were excluded from analysis through probe set selection and classified as false negatives.

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