NIDDK Central Repository - High-throughput mutation screen identifies high frequency of double and triple heterozygous gene variants in patients with idiopathic cholestasis

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NIDDK Central Repository

Publication Information

Public Release Type

Conference Presentation

Publication Year

2012

Authors

Aronow B, Bezerra J, Connor J, Dexheimer P, Karns R, Miethke A, Zhang K

Studies

PROBE

Citation

Dexheimer P, Connor J, Karns R, Miethke A, Aronow B, Zhang K, Bezerra J. High-throughput mutation screen identifies high frequency of double and triple heterozygous gene variants in patients with idiopathic cholestasis. Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. 2012.