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Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A.
Kara B, Köroğlu Ç, Peltonen K, Steinberg RC, Maraş Genç H, Hölttä-Vuori M, Güven A, Kanerva K, Kotil T, Solakoğlu S, Zhou Y, Olkkonen VM, Ikonen E, Laiho M, Tolun A. Kara B, et al. Among authors: olkkonen vm. Eur J Hum Genet. 2017 Feb;25(3):315-323. doi: 10.1038/ejhg.2016.183. Epub 2017 Jan 4. Eur J Hum Genet. 2017. PMID: 28051070 Free PMC article.
Genetic defects of intracellular-membrane transport.
Olkkonen VM, Ikonen E. Olkkonen VM, et al. N Engl J Med. 2000 Oct 12;343(15):1095-104. doi: 10.1056/NEJM200010123431507. N Engl J Med. 2000. PMID: 11027745 Review. No abstract available.
The OSBP-related protein family in humans.
Lehto M, Laitinen S, Chinetti G, Johansson M, Ehnholm C, Staels B, Ikonen E, Olkkonen VM. Lehto M, et al. Among authors: olkkonen vm. J Lipid Res. 2001 Aug;42(8):1203-13. J Lipid Res. 2001. PMID: 11483621 Free article.
225 results