Associated Papers
A Novel Silent Mutation in the L1CAM Gene Causing Fetal Hydrocephalus Detected by Whole-Exome Sequencing.
Sun Y et al.
Frontiers in Genetics, 2019
31572438 (PubMed )
Supplement: Table_1.xlsx › Sheet1
Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death.
Lin Y et al.
Journal of Electrocardiology, 0
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