A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient

alexandrossfakianakis shared this article with you from Inoreader A novel nonsense <i>PKD1L1</i> variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient via Journal of Human Genetics - Issue - nature.com science feeds Journal of Human Genetics, Published online: 13 June 2022; doi:10.1038/s10038-022-01053-w A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient View on Web

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