Associated Papers
Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders.
Nøstvik M et al.
Clinical Genetics, 2021
Compound heterozygous mutations in PUS3 gene identified in a Chinese infant with severe epileptic encephalopathy and multiple malformations.
Fang H et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
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