Mei Lu

Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.

L. Laurin, K. Weck, C. Poulton, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

A novel TRPC6 mutation in a family with podocytopathy and clinical variability

C. Fine, K. Weck, A. Mottl, 2013, BMC Nephrology.

High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting.

J. Berg, C. Bizon, Kristy Lee, 2015, American journal of ophthalmology.

The phenotype of multiple congenital anomalies‐hypotonia‐seizures syndrome 1: Report and review

J. Berg, K. Wilhelmsen, C. Powell, 2015, American journal of medical genetics. Part A.