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Olof Wålinder
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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...
by
K. Sigvard Olsson
,
Olof
Wålinder
,
Ulf Jansson
,
Maria Wilbe
,
Marie-Louise Bondeson
,
Eva-Lena Stattin
,
Ruma Raha-Chowdhury
,
Roger Williams
Published 2017-12-01
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