Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen...

por Olsson, K. Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Eva-Lena, Raha-Chowdhury, Ruma, Williams, Roger
Publicado 2017