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Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders

Author:

Anna R. Duncan,Maya M. Polovitskaya,Héctor Gaitán-Peñas,Sara Bertelli,Grace E. VanNoy,Patricia E. Grant,Anne O’Donnell-Luria,Zaheer Valivullah,Alysia Kern Lovgren,Elaina M. England,Emanuele Agolini,Jill A. Madden,Klaus Schmitz-Abe,Amy Kritzer et al.

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

5 August 2021

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