Mutation of Ala1, Asn168 and Cys+1 in MIP. Left panel: mutation

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asn168 Resmi

MEREK : asn168

Mutation of Ala1, Asn168 and Cys+1 in MIP. Left panel: mutation

asn168Glycosylation site Asn168 is important for slow in vivo clearance of recombinant human diamine oxidase heparinNM_000443.4(ABCB4):c.504C>T (p.Asn168=) AND Progressive familial intrahepatic cholestasis type 3. Germ classification: Benn (2 submissions) Last

IDR 10.000

IDR 100.000 Disc -90%

Mutation of Ala1, Asn168 and Cys+1 in MIP. Left panel: mutation

Mutation of Ala1, Asn168 and Cys+1 in MIP. Left panel: mutation

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