Publication | Open Access
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders
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Citations
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References
2021
Year
Neurodevelopmental DisordersMolecular NeuroscienceDevelopmental BiologyUnique VariantsGenetic DisorderGeneticsMolecular BiologyDisease Gene IdentificationMolecular NeurobiologyEndosomal Anion/proton ExchangerMedicineSocial SciencesNeurogenetics
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