Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations Xiaoyu Yu, Yun Lin, Jun Xu, Tuanjie Che, Lin Li, Tao Yang and Hao Wu Orphanet Journal of Rare Diseases 2020, 15:29 | Published on: 28 January 2020 Full Text | PDF RESEARCH Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain Simon Körver, Gert J. Geurtsen, Carla E. M. Hollak, Ivo N. van Schaik, Maria G. F. Longo, Marjana R. Lima, Leonardo Vedolin, Marcel G. W. Dijkgraaf and Mirjam Langeveld Orphanet Journal of Rare Diseases 2020, 15:28 | Published on: 28 January 2020 Full Text | PDF

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