Alina Esterhuizen

Publication Activity (10 Years)

Years Active: 2020-2020
Publications (10 Years): 1

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This page only lists publications with an associated author ORCID identifier.

Publications

Lisa Roberts, Stephanie Julius, Shrinav Dawlat, Safiye Yildiz, George Rebello, Surita Meldau, Komala Pillay, Alina Esterhuizen, Alvera Vorster, Gameda Benefeld, Jorge Emanuel Batista da Rocha, Peter Beighton, Sean L Sellars, Kebashni Thandrayen, John M Pettifor, Raj S Ramesar
Renal dysfunction, rod-cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B. Human mutation 41 (11) (2020)