Josef Finsterer, Fulvio A. Scorza, Carla A. Scorza
We read with interest the article by Khasawneh et al. about a 4 months-old male with Pearson syndrome due to a novel mtDNA deletion (1). We have the following comments and concerns.
[Med Arch 2018; 72(3.000): 234-236]
Keywords: Pearson Syndrome, mtDNA
>>Full text PDF >>[cite source=”doi”]10.5455/medarh.2018.72.234-236[/cite]