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Page 1
Mitochondrial hearing loss mutations among Finnish preterm and term-born infants.
Audiol Res. 2017 Nov 3;7(2):189. doi: 10.4081/audiores.2017.189. eCollection 2017 Jul 18.
Audiol Res. 2017.
PMID: 29291046
Free PMC article.
No abstract available.
Novel non-neutral mitochondrial DNA mutations found in childhood acute lymphoblastic leukemia.
Järviaho T, Hurme-Niiranen A, Soini HK, Niinimäki R, Möttönen M, Savolainen ER, Hinttala R, Harila-Saari A, Uusimaa J.
Järviaho T, et al. Among authors: soini hk.
Clin Genet. 2018 Feb;93(2):275-285. doi: 10.1111/cge.13100. Epub 2017 Dec 20.
Clin Genet. 2018.
PMID: 28708239
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Adult-onset ataxia and polyneuropathy caused by mitochondrial 8993T-->C mutation.
Rantamäki MT, Soini HK, Finnilä SM, Majamaa K, Udd B.
Rantamäki MT, et al. Among authors: soini hk.
Ann Neurol. 2005 Aug;58(2):337-40. doi: 10.1002/ana.20555.
Ann Neurol. 2005.
PMID: 16049925
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A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease.
Soini HK, Väisänen A, Kärppä M, Hinttala R, Kytövuori L, Moilanen JS, Uusimaa J, Majamaa K.
Soini HK, et al.
BMC Med Genet. 2017 Feb 10;18(1):14. doi: 10.1186/s12881-017-0377-8.
BMC Med Genet. 2017.
PMID: 28187756
Free PMC article.
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Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.
Soini HK, Moilanen JS, Vilmi-Kerälä T, Finnilä S, Majamaa K.
Soini HK, et al.
BMC Med Genet. 2013 Jul 19;14:73. doi: 10.1186/1471-2350-14-73.
BMC Med Genet. 2013.
PMID: 23870133
Free PMC article.
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Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus.
Soini HK, Moilanen JS, Finnila S, Majamaa K.
Soini HK, et al.
BMC Res Notes. 2012 Jul 10;5:350. doi: 10.1186/1756-0500-5-350.
BMC Res Notes. 2012.
PMID: 22780954
Free PMC article.
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