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Cell Press, American Journal of Human Genetics, 8(108), p. 1450-1465, 2021

DOI: 10.1016/j.ajhg.2021.06.003

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

Journal article published in 2021 by 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, Pamela Hawley and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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