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

Overview of attention for article published in American Journal of Human Genetics, June 2021

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In the top 5% of all research outputs scored by Altmetric
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news: 3 news outlets
blogs: 1 blog

twitter: 9 X users
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Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders https://t.co/BGuu9pIwyw

RT @CIBERER: 🆕Identifican dos nuevos genes implicados en enfermedades del desarrollo del #cerebro https://t.co/JA8idKE5fc Estudios👉 https…

RT @MantonCenter: Another gene discovery responsible for neurodevelopmental disorders @mantoncenter @pankajagrawalb laboratory. Unique vari…

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