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Molecular basis of glutathione reductase deficiency in human blood cells.
Kamerbeek NM, van Zwieten R, de Boer M, Morren G, Vuil H, Bannink N, Lincke C, Dolman KM, Becker K, Schirmer RH, Gromer S, Roos D. Kamerbeek NM, et al. Among authors: lincke c. Blood. 2007 Apr 15;109(8):3560-6. doi: 10.1182/blood-2006-08-042531. Epub 2006 Dec 21. Blood. 2007. PMID: 17185460 Free article.
Cerebellar hypoplasia in respiratory chain dysfunction.
Lincke CR, van den Bogert C, Nijtmans LG, Wanders RJ, Tamminga P, Barth PG. Lincke CR, et al. Neuropediatrics. 1996 Aug;27(4):216-8. doi: 10.1055/s-2007-973792. Neuropediatrics. 1996. PMID: 8892374
Tissue distribution of the human MDR3 P-glycoprotein.
Smit JJ, Schinkel AH, Mol CA, Majoor D, Mooi WJ, Jongsma AP, Lincke CR, Borst P. Smit JJ, et al. Among authors: lincke cr. Lab Invest. 1994 Nov;71(5):638-49. Lab Invest. 1994. PMID: 7734012
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis.
Vandervore LV, Schot R, Hoogeboom AJM, Lincke C, de Coo IF, Lequin MH, Dremmen M, van Unen LMA, Saris JJ, Jansen AC, van Slegtenhorst MA, Wilke M, Mancini GMS. Vandervore LV, et al. Among authors: lincke c. Eur J Med Genet. 2018 Dec;61(12):783-789. doi: 10.1016/j.ejmg.2018.10.018. Epub 2018 Oct 31. Eur J Med Genet. 2018. PMID: 30391508
22 results