Erratum: Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion

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作者：
Sanna Matilainen
Pirjo Isohanni
Liliya Euro
Tuula Lönnqvist
Helena Pihko
Tero Kivelä
Sakari Knuutila
Anu Suomalainen
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European Journal of Human Genetics | 2017年 / 25卷
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摘要：
Correction to: European Journal of Human Genetics (2015) 23, 325–330; doi:10.1038/ejhg.2014.128 The sub-heading of Table 1 is incorrect and should read:
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页数：-393
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  • [1] Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion
    Matilainen, Sanna
    Isohanni, Pirjo
    Euro, Liliya
    Lonnqvist, Tuula
    Pihko, Helena
    Kivela, Tero
    Knuutila, Sakari
    Suomalainen, Anu
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (03) : 325 - 330
  • [2] Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion
    Sanna Matilainen
    Pirjo Isohanni
    Liliya Euro
    Tuula Lönnqvist
    Helena Pihko
    Tero Kivelä
    Sakari Knuutila
    Anu Suomalainen
    European Journal of Human Genetics, 2015, 23 : 325 - 330
  • [3] Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion (vol 23, pg 325, 2015)
    Matilainen, Sanna
    Isohanni, Pirjo
    Euro, Liliya
    Lonnqvist, Tuula
    Pihko, Helena
    Kivela, Tero
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    EUROPEAN JOURNAL OF HUMAN GENETICS, 2017, 25 (03) : 393 - 393
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