Mecanismos moleculares de la enfermedad
MeMoEn
University of Oulu
Oulu, FinlandiaPublicaciones en colaboración con investigadores/as de University of Oulu (1)
2018
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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family
Brain, Vol. 141, Núm. 1, pp. 55-62