Carmen Martín Sierra-rekin lankidetzan egindako argitalpenak (2)

2017

  1. Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease

    European Journal of Human Genetics, Vol. 25, Núm. 2, pp. 200-207

2016

  1. A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease

    Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415