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Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion
Matilainen, Sanna, Isohanni, Pirjo, Euro, Liliya, Lönnqvist, Tuula, Pihko, Helena, Kivelä, Tero, Knuutila, Sakari, Suomalainen, AnuVolume:
25
Langue:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2016.166
Date:
February, 2017
Fichier:
PDF, 58 KB
english, 2017