Title : Gene Therapy for Progressive Familial Intrahepatic Cholestasis: Current Progress and Future Prospects.

Pub. Date : 2020 Dec 29

PMID : 33383947






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Six types have been reported, two of these are caused by deficiency of an ABC transporter; ABCB11 (bile salt export pump) in type 2; ABCB4 (phosphatidylcholine floppase) in type 3. Phosphatidylcholines ATP binding cassette subfamily B member 4 Homo sapiens