Title : Genetics of gallstone disease.

Pub. Date : 2018 Jul

PMID : 29635711






1 Functional Relationships(s)
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1 A smaller group of patients might develop gallstones primarily due low phosphatidylcholine concentrations in bile as a result of loss-of-function mutations of the ABCB4 transporter (low phospholipid-associated cholelithiasis syndrome). Phosphatidylcholines ATP binding cassette subfamily B member 4 Homo sapiens