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

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Bibliographic Details
Published in:European journal of human genetics : EJHG 2017-02, Vol.25 (3), p.393
Main Authors: Matilainen, Sanna, Isohanni, Pirjo, Euro, Liliya, Lönnqvist, Tuula, Pihko, Helena, Kivelä, Tero, Knuutila, Sakari, Suomalainen, Anu
Format: Article
Language:English
Online Access:Get full text
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ISSN:1018-4813
1476-5438
DOI:10.1038/ejhg.2016.166