DOI:
10.1055/s-00000069
Seminars in Liver Disease
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References
Grochowski CM, Rajagopalan R, Falsey AM. et al.
Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome.
Am J Med Genet A 2015;
167A (04) 891-893
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