Erratum: 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（2017）

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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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关键词

EJHG,human genetics,DNA diagnosis,cytogenetics,clinical genetics,molecular genetics,linkage studies

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