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

Olsson KS, Wålinder O, Jansson U, Wilbe M, Bondeson ML, Stattin EL, Raha-Chowdhury R, Williams R

Hereditas 154 (1) - [2017-12-00; online 2017-12-19]

Clinical Genomics Uppsala [Collaborative]

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DOI 10.1186/s41065-017-0052-2

Crossref 10.1186/s41065-017-0052-2