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Paper Details

Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome.
Hepatology
51
2019
2, BA, BASM, BASM syndrome, BASM) syndrome, Biliary Atresia Splenic Malformation Syndrome, Biliary atresia, Childhood Liver Disease, Children, Diabetes and Digestive and Kidney Diseases, PKD1L1, PKD1L1 variants, Polycystic Kidney Disease, Polycystic Kidney Disease 1 Like 1 Gene Variants, biliary atresia splenic malformation (, calcium, cardiac malformations, children, cholangiocyte, cholangiocyte-expressed candidate gene, cholestasis, ciliary dysgenesis and/or dysfunction, end-stage liver disease, heterotaxy, humans, infants, laterality defects, mice, patient, patients, polycystic kidney disease, polycystic kidney disease 1 like 1, splenic abnormalities
Author NameAffiliation
Aniko SaboBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
David J CutlerEmory University School of Medicine
David J CutlerEmory University School of Medicine
Nancy B SpinnerChildren's Hospital of Philadelphia
Barry MooreUniversity of Utah
Mark YandellUniversity of Utah
Mark YandellUniversity of Utah
Sanjiv HarpavatBaylor College of Medicine
Estella M AlonsoAnn and Robert H. Lurie Children's Hospital of Chicago
Philip J RosenthalUniversity of California San Francisco
Robert H SquiresChildren's Hospital of Pittsburgh of UPMC
Robert H SquiresChildren's Hospital of Pittsburgh of UPMC
Pierre RussoChildren's Hospital of Philadelphia
Ronald J SokolChildren's Hospital Colorado and University of Colorado School of Medicine
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Datasets

Release 1.2