Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Linheng Li(Stowers Institute for Medical Research), Ian D. Krantz(Children's Hospital of Philadelphia), Yu Deng(University of Washington), Anna Genin(Children's Hospital of Philadelphia), Amy B. Banta(Stowers Institute for Medical Research), Colin C. Collins(Lawrence Berkeley National Laboratory), Ming Qi(University of Washington Medical Center), Barbara J. Trask(University of Washington), Wen Lin Kuo(Cancer Research Institute), Joanne Cochran(Lawrence Berkeley National Laboratory), Teresa Costa(Hospital for Sick Children), Mary Ella Pierpont(University of Minnesota), Elizabeth B. Rand(Children's Hospital of Philadelphia), David A. Piccoli(Children's Hospital of Philadelphia), L Hood(Stowers Institute for Medical Research), Nancy B. Spinner(Children's Hospital of Philadelphia)
Nature Genetics
July 1, 1997
Cited by 1,285

Abstract


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