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pkd1l1 protein human
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Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Preventi…
Liver-restricted deletion of the biliary atresia candidate gene Pkd1l1 causes bile duct dysmorphogen…
PKD1L1 Is Involved in Congenital Chylothorax.
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese …
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidat…
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