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A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptom
7월 2, 2024
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Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families
다음:
Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneity
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