Weiliang Lu
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Mar 16, 2021
Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.Jiasun Su, Weiliang Lu, Mengting Li
|Mar 12, 2020
Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene-disease relationship.Weiliang Lu, Mingxing Liang, Jiasun Su
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