Associated Papers
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
Moteki H et al.
The Annals of Otology, Rhinology, and Laryngology, 2015
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Moteki H et al.
The Annals of Otology, Rhinology, and Laryngology, 2015