Figure 1 | European Journal of Human Genetics

Figure 1

From: An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Figure 1

Schematic representation of the large rearrangements identified at USH loci. Novel rearrangements are represented by red (deletion) or green (duplication) left-right arrows, and previously reported rearrangements are highlighted in gray. For each rearrangement, the corresponding number of USH patients from our cohort is indicated between parentheses.

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