2 results for author:"van Mil S.W.C." in Literature citations
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| Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11. van Mil S.W.C., van der Woerd W.L., van der Brugge G., Sturm E., Jansen P.L.M., Bull L.N., van den Berg I.E.T., Berger R., Houwen R.H.J., Klomp L.W.J. Gastroenterology 127:379-384(2004) · UniProtKB (1) · Mapped (4) |
| Characterization of mutations in ATP8B1 associated with hereditary cholestasis. Klomp L.W.J., Vargas J.C., van Mil S.W.C., Pawlikowska L., Strautnieks S.S., van Eijk M.J.T., Juijn J.A., Pabon-Pena C., Smith L.B., DeYoung J.A. et al. Hepatology 40:27-38(2004) · UniProtKB (1) |