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Hereditas
JSON
ISSN
1601-5223
ISSN-L
0018-0661
IUID
64dcc85ef89345379cbe846180819350
Modified
2020-11-27T13:12:56.147Z
Created
2018-12-05T12:51:33.480Z
Year 2017
PubMed
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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
Olsson KS, Wålinder O, Jansson U, ..., Raha-Chowdhury R, Williams R
Hereditas
154
(-) 16 [2017-12-19; online 2017-12-19]
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