Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland
Katarzyna Iwanicka‐Pronicka(Children's Memorial Health Institute), Maciej Pronicki(Children's Memorial Health Institute), Paulina Halat(Children's Memorial Health Institute), Dorota Piekutowska‐Abramczuk(Children's Memorial Health Institute), Elżbieta Ciara(Children's Memorial Health Institute), Magdalena Pajdowska(Children's Memorial Health Institute)
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