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Q47145435-188E2C2A-180B-46E6-842A-FDEC8B2F30C5
Q47145435-188E2C2A-180B-46E6-842A-FDEC8B2F30C5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-188E2C2A-180B-46E6-842A-FDEC8B2F30C5
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.
P2860
Q47145435-188E2C2A-180B-46E6-842A-FDEC8B2F30C5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-188E2C2A-180B-46E6-842A-FDEC8B2F30C5
rank
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Statement
wasDerivedFrom
b0ceb1986e5843e7fcc167fde79f760f0507147a
P2860
A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment.