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Q47145435-49A956DD-7A06-4F46-BBCE-0C1AF3CC2819
Q47145435-49A956DD-7A06-4F46-BBCE-0C1AF3CC2819
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-49A956DD-7A06-4F46-BBCE-0C1AF3CC2819
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.
P31
Q47145435-49A956DD-7A06-4F46-BBCE-0C1AF3CC2819
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-49A956DD-7A06-4F46-BBCE-0C1AF3CC2819
rank
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type
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Statement
wasDerivedFrom
823cb97ef770e75e83f475afdb3ef8b61fdad6a1
P31
scholarly article