Publication | Open Access
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia
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Citations
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References
2019
Year
Neurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologyMendelian DisorderBrain DevelopmentGenetic DisorderNeurodevelopmentNeuroscienceNeurologyProfound Infantile-onset HypotoniaFetal NeurodevelopmentNeurodevelopmental SyndromeMedicineAbnormal DevelopmentSocial SciencesNeurogenetics
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