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 genes
Crossref DOI link: https://doi.org/10.1186/s41065-017-0052-2
Published Online: 2017-12-19
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Olsson, K. Sigvard
Wålinder, Olof
Jansson, Ulf
Wilbe, Maria
Bondeson, Marie-Louise
Stattin, Eva-Lena
Raha-Chowdhury, Ruma
Williams, Roger
Funding for this research was provided by:
Göteborgs Läkaresällskap (GU 244003201)