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2. IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype. Issue 10 (14th August 2015)

3. Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies. Issue 3 (16th December 2015)

4. Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Issue 3 (21st March 2018)